Label: Z-BUM- diaper rash cream cream

  • NDC Code(s): 58809-375-04
  • Packager: GM Pharmaceuticals, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 26, 2024

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  • SPL UNCLASSIFIED SECTION

    Z-Bum

    NDC 58809-375-04

    4 oz. (113 grams)

  • Active ingredient

    Zinc Oxide 22%

  • Purpose

    Skin Protectant

  • Uses

    ■ helps treat and prevent diaper rash

    ■ protects chafed skin due to diaper rash and helps protect skin from wetness

  • 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

    ■ change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry.

    ■ apply cream liberally as often as necessary, with each diaper change, especially at

    bedtime or anytime when exposure to wet diapers may be prolonged.

  • Other information

    ■ store at 20-30°C (68-86°F)

  • Inactive ingredients

    aloe barbadensis leaf juice, caprylyl glycol, ceteareth- 20, cetyl alcohol, chlorphenesin, glycerine, mineral oil, petrolatum, phenoxyethanol, purified water, stearyl alcohol, tocopheryl acetate (vitamin E)

  • Questions or comments?

    Call 1-888-535-0305

    Distributed by: GM Pharmaceuticals, Inc. Fort Worth, TX 76118

  • PRINCIPAL DISPLAY PANEL

    NDC 58809-375-04

    Z-BUM

    Zinc Oxide 22% (Skin Protectant)

    Diaper Rash Cream

    Premium Protection

    Helps heal, soothe, and prevent diaper rash

    Protects chafed skin

    SOOTHING ALOE & VITAMIN E

    Gentle on sensitive skin


    NET WT 4 oz (113 grams)

    Z-Bum 2024

  • INGREDIENTS AND APPEARANCE
    Z-BUM 
    diaper rash cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58809-375
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE22 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    WATER (UNII: 059QF0KO0R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58809-375-04113 g in 1 TUBE; Type 0: Not a Combination Product12/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/01/2015
    Labeler - GM Pharmaceuticals, INC (793000860)
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