Label: 4101 FIRST AID KIT kit
4098 FIRST AID KIT kit
4099 FIRST AID KIT kit
4100 FIRST AID KIT kit
4102 FIRST AID KIT kit
4097 FIRST AID KIT kit
4103 FIRST AID KIT kit
4105 FIRST AID KIT kit
4106 FIRST AID KIT kit
4104 FIRST AID KIT kit
-
NDC Code(s):
0498-0730-01,
0498-2001-01,
0498-4097-01,
0498-4098-01, view more0498-4099-01, 0498-4100-01, 0498-4101-01, 0498-4102-01, 0498-4103-01, 0498-4104-01, 0498-4105-01, 0498-4106-01
- Packager: Honeywell Safety Products USA, INC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 22, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- First Aid Burn Cream Active ingredient
- First Aid Burn Cream Purpose
- First Aid Burn Cream Uses
- First Aid Burn Cream Warnings
- First Aid Burn Cream Directions
- First Aid Burn Cream Other information
- First Aid Burn Cream Inactive ingredients
- First Aid Burn Cream Questions
- BZK Antiseptic Wipe Active ingredient
- BZK Purpose
- BZK Uses
-
BZK
Warnings
For external use only
BZK
Do not use- in the eyes or over large areas of the body
- on mucous membranes
- on irritated skin
- in case of deep puncture wounds, animal bites or serious burns, consult a doctor
- longer than 1 week unless directed by a doctor
- BZK Directions
- BZK Other information
- BZK Inactive ingredients
- BZK Questions
- Aypanal Active igredient
- Aypanal Purpose
- Aypanal Uses
-
Aypanal
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg in 24 hours, which is the maximum daily amount - child takes
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
skin reddening
blisters
rash -
Aypanal
Directions
- do not take more than directed (see overdose warning) adults and children 12 years of age or older
- take two tablets every 4-6 hours while symptoms last
- do not take more than directed (see overdose warning)
adults and children 12 years of age or older
- take two tablets every 4-6 hours while symptoms last
- do not take more than 12 tablets in 24 hours
- children 6 to under 12 years of age
- take 1 tablet every 4-6 hours while symptoms last
- do not take more than 5 tablets in 24 hours
- children under 6 years
- consult a doctor
- Aypanal Other information
- Aypanal Inactive ingredients
- Aypanal Questions or Comments?
- Sting Relief Active ingredient
- Sting Relief Purpose
- Sting Relief Uses
- Sting Relief Warnings
- Sting Relief Directions
- Sting Relief Inactive ingredients
- Sting relief Questions or Comments
- Neomycin Antibiotic Ointment Active ingredient
- Neomycin Antibiotic Ointment Purpose
- Neomycin Antibiotic Ointment Uses
- Neomycin Antibiotic Ointment Warnings
- Neomycin Antibiotic Ointment Directions
- Neomycin Antibiotic Ointment Other information
- Neomycin Antibiotic Ointment Inactive ingredient
- Neomycin Antibiotic Ointment Questions
-
4097
019700-0001L Kit Contents
1 GAUZE PADS, 3" X 3", 4 PER
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
1 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 10 UNIT FA
1TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 WOVEN FINGERTIP BANDAGE 2" -
4098
019700-4500F Kit Contents
1 TWEEZER PLASTICS 4"
1 IRST AID GUIDE ASHI
1 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 10 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
4 GAUZE PADS 2"X2" 12PLY
1 GAUZE PADS 3"X3" 12PLY
1 WOVEN FINGERTIP BANDAGE 2" -
4099
Z019850 Kit Contents
1 TWEEZER PLASTICS 4"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
1 TAPE ADHESIVE 1/2 X 2.5 125133
1 KIT, PP 10 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY -
4100
Z019743-0030L Kit Contents
1 TWEEZER PLASTICS 4"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
1 TAPE ADHESIVE 1/2 X 2.5 125133
1 KIT, PP 16 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 EYE PADS STD OVAL STERILE
6 GAUZE PADS 3"X3" 12PLY -
4101
Z019759-0035L Kit Contents
1 GAUZE PADS, 3" X 3", 4 PER
1 ADHESIVE BDG,PLSTIC,1"X3"16PER
FLEXICON 2"X 4.1 YD 12/BAG
1 FIRST AID GUIDE ASHI
1 ABD COMBINE PAD 5" X 9"
2 BUGX TOWELETTE, BULK, 300/CS
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 TAPE ADHESIVE 1/2 X 2.5 125133
1 KIT STL 10 UN WHITE 01 -
4102
Z019742-0029L Kit Contents
1 TWEEZER PLASTICS 4"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 1 SCISSOR BDGE 4" RED PLS HDL
2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
1 TAPE ADHESIVE 1/2 X 2.5 125133
1 KIT, PP 10 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 EYE PADS STD OVAL STERILE
1 GAUZE PADS 3"X3" 12PLY -
4103
Z019701-0001L Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
1 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT STL 10 UN WHITE 01
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
4 GAUZE PADS 2"X2" 12PLY
4 GAUZE PADS 3"X3" 12PLY
1 WOVEN FINGERTIP BANDAGE 2" -
4104
Z019700-0001L Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
1 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 10 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 GAUZE PADS 2"X2" 12PLY
4 GAUZE PADS 3"X3" 12PLY
1 WOVEN FINGERTIP BANDAGE 2" -
4105
SF00004715 Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 16 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
4 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
1 GAUZE PADS 3"X3" 12PLY
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE
1 1 OZ. EYEWASH -
4106
019742-0029L Kit Contents
1 TWEEZER PLASTICS 4"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 BAGGED COMP MISC
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
1 TAPE ADHESIVE 1/2 X 2.5 125133
1 KIT, PP 10 UNIT FA
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY - First Aid Burn Cream Principal Display Panel
- BZK Principal Display Panel
- Aypanal Principal Display Panel
- Sting Relief Principal Display Panel
- Neomycin Antibiotic Ointment Principal Display Panel
- 4097 Kit Label 019700-0001L
- 4098 Kit Label 019700-4500F
- 4099 Kit Label Z019850
- 4100 Kit Lael Z019743-0030L
- 4101 Kit Label Z019759-0035L
- 4102 Kit Label Z019742-0029L
- 4103 Kit Label Z019701-0001L
- 4104 Kit Label Z019700-0001L
- 4105 Kit Label SF00004715
- 4106 Kit Label 019742-0029L
-
INGREDIENTS AND APPEARANCE
4101 FIRST AID KITÂ
4101 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4101 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4101-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  STEARIC ACID (UNII: 4ELV7Z65AP)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4098 FIRST AID KITÂ
4098 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4098 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4098-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4099 FIRST AID KITÂ
4099 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4099 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4099-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4100 FIRST AID KITÂ
4100 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4100 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4100-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 4102 FIRST AID KITÂ
4102 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4102 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4102-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4097 FIRST AID KITÂ
4097 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4097 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4097-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4103 FIRST AID KITÂ
4103 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4103 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4103-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  STEARIC ACID (UNII: 4ELV7Z65AP)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4105 FIRST AID KITÂ
4105 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4105 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4105-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4106 FIRST AID KITÂ
4106 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4106 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4106-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4104 FIRST AID KITÂ
4104 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4104 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4104-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 6 Part 2 6 POUCH 2.4 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 9 g Part 5 10 PACKET 14 mL Part 1 of 5 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 5 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 5 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 5 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 5 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 Labeler - Honeywell Safety Products USA, INC (118768815)