Label: DIAPER RASH- zinc oxide paste

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 20, 2024

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  • Active ingredients

    Zinc oxide 40%

  • Purpose

    Skin protectant

  • Uses

    • helps treat and prevent diaper rash
    • protects chafed skin due to diaper rash and helps seal out 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 soilded diapers promptly
    • cleanse the diaper area
    • allow to dry
    • apply ointment 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 between 20⁰ and 25⁰C (68⁰ and 77⁰F)

  • Inactive ingredients

    petrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance

  • Adverse Reactions 

    KEEP THIS CARTON FOR FULL PRODUCT INFORMATION

    DISTRIBUTED BY: H-E-B, SAN ANTONIO, TN 78204

    LOT NUMBER: ON PACKAGE

    QUESTIONS? 1-888-593-0593

    MADE IN USA WITH US

    AND IMPORTED COMPONENTS.

    WE HOPE YOU ARE SATISFIED WITH

    THIS PRODUCT. IF NOT, WE WILL 

    CHEERFULLY REFUND YOUR MONEY.

  • Principal display panel

    HILL COUNTRY ESSENTIALS

    Diaper Rash Paster

    SKIN PROTECTANT

    40% ZINC OXIDE

    Helps Soothe & Prevent Diaper Rash

    Pomada para Rozaduras

    PROTECTOR DE LA PIEL

    CON OXIDO DE ZINCE 40%

    FREE FROM

    • parapbens
    • phthalates
    • dyes

    NET WT. 4 OZ

    CONT. NET. 113g

    image description

  • INGREDIENTS AND APPEARANCE
    DIAPER RASH 
    zinc oxide paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE400 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    COD LIVER OIL (UNII: BBL281NWFG)  
    LANOLIN (UNII: 7EV65EAW6H)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37808-020-261 in 1 CARTON09/10/2010
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/10/2010
    Labeler - H E B (007924756)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(37808-020)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(37808-020)
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