Label: CALAMINE- ferric oxide red lotion

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 8, 2023

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  • Active ingredents

    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 within 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 59⁰-86⁰F

  • Inactive ingredients

    bentonite magma, calcium hydroxide, glycerin, purified water

  • Questions

    Call 1-800-910-6874

  • Adverse reaction

    Distributed by Target Corporation

    Minneapolis, MN 55403

    Made in U.S.A. with U.S. and foreign components

    TM & ©2024 Target Brands, Inc.

  • Principal display panel

    Calamine

    Lotion

    Calamine 8%, Zinc Oxide 8

    Skin Protectant

    Drying Treatment for Poison Ivy, Oak and Sumac

    up&up™

    6 FL OZ (177 mL)

    image description
  • INGREDIENTS AND APPEARANCE
    CALAMINE  
    ferric oxide red lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-063
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675) FERRIC OXIDE RED80 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE80 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENTONITE (UNII: A3N5ZCN45C)  
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-063-30177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/26/1997
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/26/1997
    Labeler - Target Corporation (006961700)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(11673-063)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC088520668manufacture(11673-063)
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