Label: EQUATE PAIN RELIEVER- acetaminophen tablet, film coated
- NDC Code(s): 79903-174-05, 79903-174-25, 79903-174-50
- Packager: WALMART INC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 20, 2024
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- 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
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- more than 4,000 mg of acetaminophen in 24 hours
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- with other drugs containing acetaminophen
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- 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
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- skin reddening
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- blisters
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- rash
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
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- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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- if you have ever had an allergic reaction to this product or any of its ingredients
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Directions
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- do not take more than directed (see overdose warning)
Adults and children 12 years and over:
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- take 2 caplets every 6 hours while symptoms last
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- do not take more than 6 caplets in 24 hours, unless directed by a doctor
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- do not use for more than 10 days unless directed by a doctor
Children under 12 years: ask a doctor
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
EQUATE PAIN RELIEVER
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-174 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 CARNAUBA WAX (UNII: R12CBM0EIZ) STARCH, CORN (UNII: O8232NY3SJ) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color WHITE Score no score Shape OVAL Size 18mm Flavor Imprint Code L24K Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-174-25 250 in 1 BOTTLE; Type 0: Not a Combination Product 01/11/2023 2 NDC:79903-174-50 2 in 1 PACKAGE 01/11/2023 2 250 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:79903-174-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 05/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 01/11/2023 Labeler - WALMART INC. (051957769)