Label: ACETAMINOPHEN tablet
- NDC Code(s): 41415-538-05, 41415-538-10
- Packager: PUBLIX SUPERMARKETS, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each coated tablet)
- Purpose
- Uses
- Liver warning:
- Allergy alert:
- Do not use
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children
-
Directions
■ do not take 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 information
- Inactive ingredients
- Questions or comments?
- Principal display panel
-
INGREDIENTS AND APPEARANCE
ACETAMINOPHEN
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41415-538 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) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE K30 (UNII: U725QWY32X) SUCRALOSE (UNII: 96K6UQ3ZD4) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color red Score no score Shape ROUND Size 11mm Flavor Imprint Code L;1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41415-538-05 50 in 1 BOTTLE; Type 0: Not a Combination Product 09/09/2024 2 NDC:41415-538-10 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/09/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 09/09/2024 Labeler - PUBLIX SUPERMARKETS, INC (006922009)