Label: MAX RELIEF JUNIOR GRAPE- children acetaminophen suspension

  • NDC Code(s): 71399-0048-4, 71399-0048-6, 71399-0048-8
  • Packager: Akron Pharma Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 28, 2024

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

  • Active Ingredient

    Active ingredient (in each 5mL)                                            Purpose
    Acetaminophen 160 mg ………………………….........Pain reliever/fever reducer

  • Uses

    temporarily: reduces fever

    relieves minor aches and pains due to:

    • the common cold
    • flu
    • headache
    • sore throat
    • toothache
  • Warnings

    Liver Warning: This product contains acetaminophen. Severe liver damage may occur if your child takes:

    • more then 5 doses in 24 hours, which is the maximum daily amount
    • with other drugs containing acetaminophen

    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.

    Sore throat warning: 

    if sore throat is severe, persist or more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

    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 your child is allergic to acetaminophen or anyof the inactive ingredients in this product.

    Ask a doctor or pharmacist before use if the child has

    liver disease.

    Ask  doctor or pharmacist before use if your child is 

    taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning)

    Stop use and ask a doctor if

    • pain gets worse or lasts for more then 5 days
    • fever gets worse or last for more then 3 days
    • new symptoms occur redness or swelling is present. These could be signs of a serious condition. 

    Overdose warning:

    In case of overdose, get medical help to contact Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical even if you do not notice any signs or symptoms.

    Keep out of Reach of children

  • Directions

    • this product does not contain directions or complete warnings for adult use
    • shake well before using
    • mL = milliliter
    • find right dose on chart below. if possible, use weight to dose, otherwise use age 
    • use only the enclosed dosing cup designed for use with product.
     Weight (lbs) Age (yrs.) Dose (tsp or mL)Weight (lbs)  Age (yrs.)Dose (tsp or mL) 
     under 24 under 2 ask a doctor 48 to 59 6 to 8 2 tsp or 10 mL
     25 to 35 2 to 3 1 tsp or 5 mL 60 to 71 9 to 10 2 1/2 tsp or 12.5 mL
     36 to 47 4 to 5 1 1/2 tsp or 7.5 mL 72 to 95 11 2 1/2 tsp or 12.5 mL

  • Other Information

    • Store at room temperature 20°-25°C (68°-77°F). Protect from freezing. Protect from light.
  • Inactive Ingredients

    Anhydrous Citric Acid, Grape Flavor, Glycerin, Microcrystalline cellulose and Sodium Methyl Cellulose, Potassium Sorbate, Purified Water, Sorbitol, Sucralose, Sucrose, Xanthan gum.

  • Questions or comments?

    call toll-free 1-877-225-6999

    Manufactured for:

    Akron Pharma, Inc.

    Fairfield, NJ 07004

    www.akronpharma.com

  • PRINCIPAL DISPLAY PANEL

    4OZ

    4OZ-CT

    8OZ

    8OZ-CT

    16OZ

  • INGREDIENTS AND APPEARANCE
    MAX RELIEF JUNIOR GRAPE 
    children acetaminophen suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0048
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN160 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71399-0048-41 in 1 CARTON04/24/2024
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:71399-0048-81 in 1 CARTON04/24/2024
    2236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:71399-0048-6473 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01304/24/2024
    Labeler - Akron Pharma Inc. (067878881)