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FeverALL Junior (Actavis Mid Atlantic LLC)

Available Formats

Dosage Form Package Information Links
SUPPOSITORY 6 SUPPOSITORY in 1 BOX (0472-1202-06) Label Information
SUPPOSITORY 50 SUPPOSITORY in 1 BOX (0472-1202-50) Label Information

Complete FeverALL Junior Information

  • ACTIVE INGREDIENT

    Acetaminophen, USP 325 mg


  • PURPOSES

    Pain reliever/fever reducer


  • USES

    Temporarily

    • reduces fever
    • relieves minor aches, pains, and headache

  • WARNINGS

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if

    • a child 6 to 12 years takes more than 5 doses in 24 hours
    • an adult or child 12 years and older takes more than 6 doses in 24 hours, which is the maximum daily amount
    • taken with other drugs containing acetaminophen
    • an adult takes 3 or more alcoholic drinks everyday 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.

    For rectal use only


  • DO NOT USE

    • in children under 6 years
    • if you are allergic to acetaminophen.
    • with any other drug containing acetaminophen (prescription or nonprescription).  If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist

  • ASK A DOCTOR BEFORE USE IF

    • you have liver disease.
    • you are taking the blood thinning drug warfarin.

  • STOP USE AND ASK A DOCTOR IF

    • fever lasts more than 3 days (72 hours), or recurs.
    • pain gets worse  or lasts more than 10 days.
    • new symptoms occur.
    • redness or swelling is present in the painful area.

    These may 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

    If swallowed or in case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical in case of overdose for adults and for children even if you do not notice any signs or symptoms.


  • DIRECTIONS

    • do not use more than directed
    • remove wrapper
    • carefully insert suppository well up into the rectum
     Dosing Chart
     Age  Dose
     under 6 years  do not use
     6 to 12 years  Use 1 suppository every 4 to 6 hours (maximum of 5 doses in 24 hours)
     adults and children 12 years and older  Use 2 suppositories every 4 to 6 hours (maximum of 6 doses)

    Other information

    • store at 2º-27ºC (35º-80ºF)
    • do not use if imprinted suppository wrapper is opened or damaged

  • INACTIVE INGREDIENTS

    Glycerol monostearate, hydrogenated vegetable oil, polyoxyethylene stearate, polysorbate 80


  • QUESTIONS

    1-800-432-8534 between 9 am and 4 pm EST, Monday – Friday.


  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Jr. Strength

    Ages 6-12 years

    325 mg

    NDC 0472-1202-06

    FeverAll®

    Acetaminophen Suppositories

    Pain reliever/fever reducer

    6 Rectal Suppositories

    325 mg each

    9d0fc82f-figure-02

    6 RECTAL SUPPOSITORIES CARTON LABEL


  • INGREDIENTS AND APPEARANCE
    FEVERALL JUNIOR 
    acetaminophen suppository
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0472-1202
    Route of Administration RECTAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0472-1202-06 6 in 1 BOX
    2 NDC:0472-1202-50 50 in 1 BOX
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018337 04/01/1980
    Labeler - Actavis Mid Atlantic LLC (809515898)
    Establishment
    Name Address ID/FEI Business Operations
    Actavis Mid Atlantic LLC 809515898 ANALYSIS(0472-1202) , LABEL(0472-1202) , MANUFACTURE(0472-1202) , PACK(0472-1202)