Label: ACETAMINOPHEN tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 31, 2022

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  • ACTIVE INGREDIENT

    Actives

  • ASK DOCTOR

    Ask a Doctor

  • ASK DOCTOR/PHARMACIST

    Ask a Doc or Pharm

  • DO NOT USE

    Do not Use

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • PREGNANCY OR BREAST FEEDING

    Pregnancy

  • PURPOSE

    Purpose

  • QUESTIONS

    Questions

  • STOP USE

    Stop Use

  • WHEN USING

    Directions when using

  • OVERDOSAGE

    Overdose

  • WARNINGS

    Warnings

  • INDICATIONS & USAGE

    Uses

  • INACTIVE INGREDIENT

    Inactives

  • STORAGE AND HANDLING

    Storage and Handling

  • DOSAGE & ADMINISTRATION

    Directions

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    ACETAMINOPHEN 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69732-002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeROUNDSize8mm
    FlavorImprint Code H325
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69732-002-0130 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34304/30/2020
    Labeler - Hi-Tech Nutraceuticals, LLC (606221443)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hi-Tech Nutraceuticals, LLC080787135pack(69732-002)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hi-Tech Nutraceuticals, LLC606221443manufacture(69732-002)