Label: ALCOHOL WIPE- isopropyl alcohol swab
ALCOHOL PREP PAD- isopropyl alcohol swab
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NDC Code(s):
0498-0142-34,
0498-0143-04,
0498-0143-05,
0498-0143-10, view more0498-0143-33, 0498-0143-34
- Packager: Honeywell Safety Products USA, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 12, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredient
- Questions
- alcohol wipes
- Alcohol wipes 10 ct
- OH Pak
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INGREDIENTS AND APPEARANCE
ALCOHOL WIPE
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-0143 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0143-04 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 09/18/2018 2 NDC:0498-0143-34 10 in 1 BOX 09/18/2018 2 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:0498-0143-05 50 in 1 BOX 09/18/2018 3 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 4 NDC:0498-0143-10 100 in 1 BOX 09/18/2018 4 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 5 NDC:0498-0143-33 3000 in 1 BOX 09/18/2018 5 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 09/18/2018 ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-0142 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0142-34 10 in 1 BOX 01/01/2017 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 01/01/2017 Labeler - Honeywell Safety Products USA, Inc (118768815) Registrant - Honeywell Safety Products USA, Inc (118768815)