Label: GENCARE- PAIN RELIEF ACETAMINOPHEN- acetaminophen tablet

  • NDC Code(s): 72090-069-01
  • Packager: Pioneer Life Sciences, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 12, 2026

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

  • Active ingredient (in each tablet)

    Acetaminophen 325 mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

    ■ temporarily relieves 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. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. 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, which is the maximum daily amount

    ■ 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
    ■ blistersmm

    ■ rash
    If a skin reaction occurs, stop use and seek medical help right away.

  • DO NOT USE

    Do not use

    ■ with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

    ■ if you are allergic to acetaminophen or any of the inactive ingredients in this product

  • ASK DOCTOR

    Ask a doctor before use if the user has liver disease

  • ASK DOCTOR/PHARMACIST

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

  • STOP USE

    Stop use and ask a doctor if

    ■ pain gets worse or lasts more than 10 days in adults

    ■ pain gets worse or lasts more than 5 days in children under 12 years

    ■ 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.

  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    Overdose warning: In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. 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 and 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, unless directed by a doctor
    ■ do not use for more than 10 days unless directed by a doctor
     children 6 years to under 12 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
     children under 6 years ask a doctor

  • Other information

    ■ store between 20° to 25°C (68° to 77°F)

  • Inactive ingredients

    hypromellose-5, hypromellose-15, magnesium stearate, microcrystalline cellulose, polyethylene glycol-400, polyvinyl pyrrolidone, pregelatinized starch, stearic acid powder, talc, titanium dioxide

  • Questions or comments?

    Call +1 (732) 994-2808 or email: support@gencare.health

  • SPL UNCLASSIFIED SECTION

    †This product is neither manufactured nor distributed by Kenvue Brands LLC, owner of the registered trademark TYLENOL®.

    Distributed by: Gencare Consumer Products, LLC 40E Cotters Ln, Suite A, East Brunswick, NJ 08816 www.gencare.health

  • NDC 72090-069-01

    L187-00-00 GC Pain Relief

  • INGREDIENTS AND APPEARANCE
    GENCARE- PAIN RELIEF ACETAMINOPHEN 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72090-069
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) Acetaminophen325 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TALC (UNII: 7SEV7J4R1U)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code S99
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72090-069-011000 in 1 BOTTLE; Type 0: Not a Combination Product08/12/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01308/12/2026
    Labeler - Pioneer Life Sciences, LLC (014092742)
    Registrant - Pioneer Life Sciences, LLC (014092742)