Label: ACETAMINOPHEN tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 69732-002-01 - Packager: Hi-Tech Nutraceuticals, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 6, 2026
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- PURPOSE
- QUESTIONS
- STOP USE
- WHEN USING
- OVERDOSAGE
- WARNINGS
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- STORAGE AND HANDLING
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACETAMINOPHEN
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69732-002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) MAGNESIUM STEARATE (UNII: 70097M6I30) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 8mm Flavor Imprint Code H325 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69732-002-01 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 04/30/2020 Labeler - Hi-Tech Nutraceuticals, LLC (606221443) Establishment Name Address ID/FEI Business Operations Hi-Tech Nutraceuticals, LLC 080787135 pack(69732-002) Establishment Name Address ID/FEI Business Operations Hi-Tech Nutraceuticals, LLC 606221443 manufacture(69732-002)
