Label: ACETAMINOPHEN tablet

  • NDC Code(s): 71335-2747-0, 71335-2747-1, 71335-2747-2, 71335-2747-3, view more
    71335-2747-4, 71335-2747-5, 71335-2747-6, 71335-2747-7, 71335-2747-8, 71335-2747-9
  • Packager: Bryant Ranch Prepack
  • This is a repackaged label.
  • Source NDC Code(s): 71399-1025
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 2, 2025

If you are a consumer or patient please visit this version.

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  • Active ingredient (in each tablet)

    Acetaminophen 325 mg

  • Purpose

    Pain Reliever/Fever Reducer

  • Uses

    To reduce fever and for the temporary relief of minor aches and pains due to:

    •headache

    •muscular aches

    •backache

    •minor pain of arthritis

    •the common cold

    •toothache

    •premenstrual and menstrual cramps.

    •Temporarily reduces fever.

  • Warnings

    Liver warning:

    This product contains acetaminophen. Severe liver damage may occur if 

    • adult takes more than 4,000 mg of acetaminophen in 24 hours
    • child takes more than 5 doses in 24 hours 
    • taken with other drugs containing acetaminophen 
    • adult has 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

    • with any other drug containing acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if the user has ever had an allergic reaction to this product or any of its ingredients.

    Ask a doctor before use if the user has

    • has liver disease
    • is a child with pain of arthritis

    Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin

    Stop use and ask a doctor if:

    • pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present.

    These could be signs of a serious condition.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children.

    Overdose Warning:

    Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

    Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions - do not take more than directed (see overdose warning)

     adults & children
    12 years and over
    • take 2 tablets every 4 to 6 hours while symptoms last
    • do not take more than 10 tablets in 24 hours
    • do not use for more than 10 days unless directed by a doctor
     children 6-11 years
    •  take 1 tablet every 4 to 6 hours while symptoms last
    • do not take more than 5 tablets in 24 hours
    • do not use for more than 5 days unless directed by a doctor
     child under 6 years ask a doctor

  • Other information

    • store at 20° to 25°C (68° to 77°F)
  • Inactive Ingredients:

    Gelatinized starch, magnesium stearate, povidone

  • Questions or Comments?

    Call toll-free 1-877-225-6999

    Manufactured for
    Akron Pharma, Inc.,

    373 RT US46 W Building E,

    Suite 117, Fairfeld, NJ - 07004

    Mfg. Lic. No: TN/DRUGS/558/1997

    * This product is not manufactured or distributed by Johnson and Johnson, consumer inc., distributor of regular Tylenol Tablets.

  • HOW SUPPLIED

    Acetaminophen 325 mg tablet: white color, round shape and the imprint code is A325. 

    NDC: 71335-2747-1: 20 Tablets in a BOTTLE

    NDC: 71335-2747-2: 100 Tablets in a BOTTLE

    NDC: 71335-2747-3: 30 Tablets in a BOTTLE

    NDC: 71335-2747-4: 2 Tablets in a BOTTLE

    NDC: 71335-2747-5: 6 Tablets in a BOTTLE

    NDC: 71335-2747-6: 10 Tablets in a BOTTLE

    NDC: 71335-2747-7: 60 Tablets in a BOTTLE

    NDC: 71335-2747-8: 90 Tablets in a BOTTLE

    NDC: 71335-2747-9: 40 Tablets in a BOTTLE

    NDC: 71335-2747-0: 24 Tablets in a BOTTLE

    Store at 20° to 25°C (68° to 77°F)

    Repackaged/Relabeled by:
    Bryant Ranch Prepack, Inc.
    Burbank, CA 91504

  • PRINCIPAL DISPLAY PANEL

    Acetaminophen 325 mg Tablet

    Label
  • INGREDIENTS AND APPEARANCE
    ACETAMINOPHEN 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-2747(NDC:71399-1025)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    Product Characteristics
    ColorwhiteScore2 pieces
    ShapeROUNDSize4mm
    FlavorImprint Code A325
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71335-2747-120 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    2NDC:71335-2747-2100 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    3NDC:71335-2747-330 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    4NDC:71335-2747-42 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    5NDC:71335-2747-56 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    6NDC:71335-2747-610 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    7NDC:71335-2747-760 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    8NDC:71335-2747-890 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    9NDC:71335-2747-940 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    10NDC:71335-2747-024 in 1 BOTTLE; Type 0: Not a Combination Product10/02/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01312/06/2024
    Labeler - Bryant Ranch Prepack (171714327)
    Registrant - Bryant Ranch Prepack (171714327)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bryant Ranch Prepack171714327REPACK(71335-2747) , RELABEL(71335-2747)
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