Label: ACETAMINOPHEN tablet
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NDC Code(s):
55319-177-05,
55319-177-10,
55319-177-24,
55319-177-25, view more55319-177-50
- Packager: FAMILY DOLLAR
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
- Uses
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Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
■ more than 4,000 mg of acetaminophen in 24 hours
■ 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 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
- Overdose warning:
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Directions
■ do not take more than directed (see overdose warning)
adults and children 12 years and over
■ take 2 caplets every 6 hours while symptoms last
■ do not take more than 6 caplets in 24 hours, unless directed by a doctor
■ do not use for more than 10 days unless directed by a doctorchildren under
12 years ■ ask a doctor - Other information
- Inactive ingredients
- Questions or comments?
- Pricipal Display Panel
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INGREDIENTS AND APPEARANCE
ACETAMINOPHEN
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-177 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 HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE K30 (UNII: U725QWY32X) STARCH, CORN (UNII: O8232NY3SJ) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white (WHITE TO OFF-WHITE) Score no score Shape CAPSULE Size 17mm Flavor Imprint Code G;551 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55319-177-24 24 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2023 2 NDC:55319-177-05 50 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2023 3 NDC:55319-177-10 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2023 4 NDC:55319-177-25 250 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2023 5 NDC:55319-177-50 500 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 09/01/2023 Labeler - FAMILY DOLLAR (024472631)