Label: ZEE PAIN AID- acetaminophen salicylamide aspirin tablet

  • NDC Code(s): 42961-042-01, 42961-042-02, 42961-042-03, 42961-042-04
  • Packager: Cintas Corporation
  • Category: HUMAN OTC DRUG LABEL

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 January 5, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredient/TabletAcetaminophen 110mg, Aspirin 162 mg-Salicylamide 152 mg,Pain Reviever Aid, Caffeine 32.5 mg-Pain Reliever Aid

  • PURPOSE

    Purpose-Pain Reliever/Fever Reducer

  • INDICATIONS & USAGE

    Temporarily relieves pain dut to: headache, muscular aches, cold, flu.  Temporarily reduces fever

  • DOSAGE & ADMINISTRATION

    Adults: Take 2 caplets every 6 hours, not to exceed 8 caplets in 24 hours

    Children under 12 years, ask a doctor


  • WARNINGS

    Liver Warning: This product contains acetaminophen. Severe liver damage
         may occur if you take:
    •    more than 8 tablets in 24 hours
    •    with other drugs containing acetaminophen (prescription or nonprescription).  Ask a doctor or pharmacist before using with other drugs if you are not sure.  
    •    3 or more alcoholic drinks every day while using this product
    ______________________________________________________________
    Do not use:
    •    with any other product containing acetaminophen this will provide more  
    than the recommended dose (overdose) of acetaminophen and could  
    cause serious health concerns.  
    •    for more than 10 days for pain unless directed by a doctor
    •    for more than 3 days for fever unless directed by a doctor
    •    When using this product do not exceed recommended dose.
    _______________________________________________________________
    Stop use and ask a doctor if:
    •    symptoms do not improve
    •    pain or fever persists or gets worse
    •    new symptoms occur
    •    redness or swelling is present

  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. In case of overdose,  
    get medical help or contact a Poison Control Center right away.  
    Prompt medical attention is critical for adults as well as for  
    children even if you do not notice any signs or symptoms.

  • INACTIVE INGREDIENT

    Inactive Ingredients: corn starch, microcrystalline cellulose,  
    povidone,  croscarmellose sodium, FDC Yellow 6, magnesium stearate, and stearic acid

  • PRINCIPAL DISPLAY PANEL

    PainAid, 250 Box PainAid, 250 Box

  • INGREDIENTS AND APPEARANCE
    ZEE PAIN AID 
    acetaminophen salicylamide aspirin tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-042
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN110 mg
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN162 mg
    SALICYLAMIDE (UNII: EM8BM710ZC) (SALICYLAMIDE - UNII:EM8BM710ZC) SALICYLAMIDE152 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    Product Characteristics
    Colororange (light orange) Scoreno score
    ShapeROUND (PA;ZEE) Size11mm
    FlavorImprint Code PA;ZEE
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42961-042-04500 in 1 CARTON01/05/2021
    1NDC:42961-042-0350 in 1 CARTON
    1NDC:42961-042-02125 in 1 CARTON
    1NDC:42961-042-012 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34301/05/2021
    Labeler - Cintas Corporation (056481716)
    Registrant - Cintas Corporation (056481716)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ultratab Laboratories, Inc.151051757manufacture(42961-042)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ultra Seal Corporation085752004pack(42961-042)