Home > Drugs A-Z > Calamine

Calamine (Dolgencorp, LLC)

Available Formats

Dosage Form Package Information Links
LOTION .177 L in 1 TUBE (55910-063-30) Label Information

Complete Calamine Information

  • Active ingredients

    Calamine 8%
    Zinc oxide 8%


  • Purpose

    skin protectant


  • Use

    dries the oozing and weeping of poison:ivy oak sumac


  • Warnings

    For external use only


  • When using this product

    do not get into eyes


  • Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again wthin a few days

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away


  • Directions

    shake well before using apply as needed


  • Other information

    store at 59⁰ - 86⁰ F


  • Inactive ingredients

    bentonite magma, calcium hydroxide, glycerin, purified water


  • SPL UNCLASSIFIED SECTION

    Visit us at: Rexall.com
    or call 1-866-4REXALL

    DISTRIBUTED BY DOLGENCORP, LLC
    100 MISSION RIDGE
    GOODLETTSVILLE, TN 37072 USA

    063.001/063AA


  • Principal Display Panel

    Since 1903
    REXALL

    Calamine Lotion
    Calamine Topical Suspension USP
    Poison ivy, oak and sumac drying lotion
    Skin protectant

    6 FL OZ (177 mL)

    image description


  • INGREDIENTS AND APPEARANCE
    CALAMINE  
    ferric oxide red lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-063
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675) FERRIC OXIDE RED 8 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 8 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    bentonite (UNII: A3N5ZCN45C)  
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55910-063-30 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/13/2009
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 04/13/2009
    Labeler - Dolgencorp, LLC (068331990)
    Registrant - Vi Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi Jon 790752542 manufacture(55910-063)