Label: MCKESSON SKIN PROTECTANT- zinc oxide cream

  • NDC Code(s): 68599-5312-1, 68599-5312-2, 68599-5312-6
  • Packager: McKesson Medical-Surgical Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 11, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredient

    Zinc Oxide 5.0%

  • PURPOSE

    Purpose

    Anorectal

  • INDICATIONS & USAGE

    Uses

    Provides temporary relief of itching and discomfort in the perineal area

  • WARNINGS

    Warnings

    For external use only.

    If condition worsens or does not improve within 7 days, consult a physician

    Do not exceed the recommended daily dosage unless directed by a physician

    In case of bleeding, consult a physician immediately

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    When practical, clean the affected area by patting or blotting with an appropriate cleaning pad.

    Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.

    Apply Skin Protectant Cream externally to affected area.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Purified Water, Cyclotetrasiloxane, Isopropyl Palmitate, Ethylhexyl Palmitate, Glycerin, Cyclopentasiloxane, Polyglyceryl-4 Isostearate,
    Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Cetyl Dimethicone, Dimethicone, Tocopherol (Vitamin E), Zea Mays Oil, Retinyl Palmitate (Vitamin A), Cholecalciferol (Vitamin D3), Beeswax, Hydrogenated Castor Oil, Sodium Chloride, DMDM Hydantoin, Iodopropynyl Butylcarbamate

  • QUESTIONS

    Questions? Call 1-800-777-4908

  • PRINCIPAL DISPLAY PANEL

    NDC 68599-5312-6

    McKesson

    Skin

    Protectant

    Cream

    Contains Zinc Oxide

    with Vitamins A, D, and E

    NET CONTENTS

    6 oz

    (177 ml)

    MFR # 53-23103

    53-23103 Each

  • INGREDIENTS AND APPEARANCE
    MCKESSON SKIN PROTECTANT 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-5312
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CORN OIL (UNII: 8470G57WFM)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 4 (UNII: CZ227117JE)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
    HEXYL LAURATE (UNII: 4CG9F9W01Q)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-5312-124 in 1 CASE10/25/201801/16/2019
    1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:68599-5312-224 in 1 CASE10/25/201801/16/2019
    2207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:68599-5312-624 in 1 CASE10/25/2018
    3117 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01604/24/2014
    Labeler - McKesson Medical-Surgical Inc. (023904428)
    Establishment
    NameAddressID/FEIBusiness Operations
    Central Solutions007118524manufacture(68599-5312)