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QUALITY CHOICE EXTRA STRENGTH ANTI ITCH (CHAIN DRUG MARKETING ASSOCIATION INC)

Available Formats

Dosage Form Package Information Links
CREAM 1 TUBE in 1 CARTON (63868-947-30) > 30 g in 1 TUBE Label Information

Complete QUALITY CHOICE EXTRA STRENGTH ANTI ITCH Information

  • ACTIVE INGREDIENT

    Active Ingredients                                                                               Purpose

    Diphenhydramine hydrochloride USP, 2%.............................................Antihistamine

    Zinc acetate, 0.1%.............................................................................Skin protectant


  • PURPOSE

    Uses

    • for the temporary relief of itching and pain associated with minor skin irritations and rashes due to insect bites, poison ivy, poison oak, and poison sumac
    • dries the oozing and weeping of poison ivy, poison oak and poison sumac

  • WARNINGS

    Warnings

    For external use only


  • DO NOT USE

    Do not use

    • on chicken pox, measles, sunburn, oozing skin, broken blisters or on extensive areas of the skin more than directed
    • any other drug containing diphenhydramine while using this product

  • WHEN USING

    When using this product avoid contact with the eyes


  • STOP USE

    Stop use and ask a doctor if condition worsens, or if symptoms persists for more than 7 days, or clear up and occur again within a few days


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away


  • INDICATIONS & USAGE

    Directions

    • adults and children 12 years of age and older,apply to affected area not more than 3 to 4 times daily, or as directed by a doctor
    • children under 12 years of age, consult a doctor

  • STORAGE AND HANDLING

    Other information

    • store at room temperature
    • Lot No. and Exp. Date: see box or see crimp of tube

  • INACTIVE INGREDIENT

    Inactive ingredients

    glycerin, sodium chloride, petrolatum, cetyl alcohol, dimethicone, isopropyl palmitate, distearyldimodium chloride (1-Octadecanaminium, N, N-Dimmethyl-N-Octadecyl-Chloride), methylparaben, propylparaben, purified water, hydroxyethyl cellulose


  • DOSAGE & ADMINISTRATION

    DISTRIBUTED BY QUALITY CHOICE

    NOVI, MI 48376-0995

    MADE IN KOREA

    QC 94731

    www.chaindrug.com


  • PRINCIPAL DISPLAY PANEL

    image of carton labelEnter section text here


  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE EXTRA STRENGTH ANTI ITCH 
    diphenhydramine hydrochloride, zinc acetate cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-947
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 2 g  in 100 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC - UNII:J41CSQ7QDS) ZINC ACETATE 0.1 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63868-947-30 1 in 1 CARTON
    1 30 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part336 02/13/2012
    Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)