Label: NORTEMP- acetaminophen solution/ drops

  • 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 December 20, 2013

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  • Drug Facts

    Active Ingredient: Acetaminophen 80 mg (in each 0.8 mL)

  • PURPOSE

    Purpose: Fever reducer/pain reliever

  • Uses

    temporarily:

    ■ reduces fever

    ■ relieves minor aches and pains due to: ■ the common cold ■ flu ■ headaches ■ sore throat  ■ toothaches

  • Warnings

    Liver warning:This product contains acetaminophen. Severe liver damage may occur if your child takes: ■ more than 5 doses in 24 hours, which is the maximum daily amount ■ with other drugs containing acetaminophen

    Sore throat warning: if sore throat is severe, persists for 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 any of the inactive ingredients in this product

    Ask a doctor before use if your child has liver disease.

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

  • When using this product

    • do not exceed recommended dosage. (see overdose warning)
  • Stop use and ask a doctor if

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

  • KEEP OUT OF REACH OF CHILDREN

    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 even if you do not notice any signs or symptoms.

  • Directions

    ■ this product does not contain directions or complete warnings for adult use ■ do not give more than directed (see overdose warning) ■ find right dose chart, if possible use weight to dose; otherwise, use age ■ use only enclosed dropper designed for use with this product, do not use any other dosing device ■ fill to dose level ■dispense liquid slowly into child's mouth, toward inner cheek ■ may be given alone or mixed with formula, milk, juice etc. ■if needed repeat dose every 4 hours ■do not give more than 5 times in 24 hours ■ Replace dropper tightly to maintain child resistance

    Weight (lb)Age (yr)Dose (mL)
    Under 24
    under 2 years
    Ask a Doctor
    24-35
    2-3 years
    1.6 mL (0.8mL +0.8mL)

    For accurate dosing follow dosing instructions using the enclosed dropper. Fill dropper to 0.8 mL or prescribed level, and dispense with a single firm squeeze of the dropper bulb

    Other information
    Store between 20°-25°C (68°-77°F)

  • Inactive ingredients

    citric acid, FD&C yellow no. 6, cherry flavor, methylparaben, saccharin sodium, sodium benzoate, sodium citrate, propylene glycol and purified water.

  • Comments

    1-800-847-1921

    Manufactured for:

    BallayPharmaceuticals, Inc.
    200 Stillwater St.
    Wimberley , TX 78676

  • PRINCIPAL DISPLAY PANEL


    Carton


  • INGREDIENTS AND APPEARANCE
    NORTEMP 
    acetaminophen solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63162-518
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen80 mg  in 0.8 mL
    Inactive Ingredients
    Ingredient NameStrength
    anhydrous citric acid (UNII: XF417D3PSL)  
    FD&C yellow no. 6 (UNII: H77VEI93A8)  
    methylparaben (UNII: A2I8C7HI9T)  
    saccharin sodium dihydrate (UNII: SB8ZUX40TY)  
    sodium benzoate (UNII: OJ245FE5EU)  
    sodium citrate (UNII: 1Q73Q2JULR)  
    propylene glycol (UNII: 6DC9Q167V3)  
    water (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRY (wild cherry) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63162-518-3030 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34304/01/1997
    Labeler - Ballay Pharmaceuticals, Inc (035888200)