Label: GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN- acetaminophen tablet
GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN- acetaminophen tablet, film coated
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NDC Code(s):
47682-170-33,
47682-170-48,
47682-170-99,
47682-619-33, view more47682-619-48, 47682-619-99
- Packager: Unifirst First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
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
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
If a skin reaction occurs, stop use and seek medical help right away.
- DO NOT USE
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
do not use more than directed (see overdose warning)
Adults and children (12 years and over)
- take 2 tablets every 6 hours while symptoms last.
- do not take more than 6 tablets in 24 hours, unless directed by a doctor
- do not use for more than 10 days unless directed by a doctor
Children under 12 years: Ask a doctor
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
Maximum Strength Non-Aspirin relief
Acetaminophen 500 mg/Acetaminofeno 500 mg
Pain Reliever/Fever Reducer
Alivia el Dolor/Reduce la Fiebre
Compare Active Ingredient To Extra Strength Tylenol®
Green Guard®
Pull Out
Tire Para Abrir
Tylenol® is a Registered Trademark of McNeil Consumer Products
50 Packets of 2 Tablets
100 Tablets
Order #2224
Distributed by Green Guard® St Louis. MO 63045
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INGREDIENTS AND APPEARANCE
GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-170 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape ROUND Size 12mm Flavor Imprint Code 44;148 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-170-33 50 in 1 BOX 02/01/2023 1 NDC:47682-170-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-170-48 125 in 1 BOX 02/01/2023 2 NDC:47682-170-99 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 OTC Monograph Drug M013 02/01/2023 GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-619 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STEARIC ACID (UNII: 4ELV7Z65AP) STARCH, CORN (UNII: O8232NY3SJ) POVIDONE K30 (UNII: U725QWY32X) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Product Characteristics Color white ((white to off white)) Score no score Shape ROUND Size 12mm Flavor Imprint Code G552 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-619-33 50 in 1 CARTON 02/06/2024 1 NDC:47682-619-99 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-619-48 125 in 1 CARTON 02/06/2024 2 NDC:47682-619-99 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 OTC Monograph Drug M013 02/06/2024 Labeler - Unifirst First Aid Corporation (832947092) Establishment Name Address ID/FEI Business Operations Prestige Packaging 080667761 pack(47682-170, 47682-619) Establishment Name Address ID/FEI Business Operations Medique Products 086911794 pack(47682-170, 47682-619)