Label: AKIN DIAPER RASH- zinc oxide cream

  • NDC Code(s): 69822-003-06
  • Packager: Southern Sales & Service, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 29, 2023

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  • Drug Facts

  • Active ingredients

    Zinc Oxide 5.0%

  • Purpose

    Skin Protectant

  • Uses

    • Helps treat and prevent diaper rash
    • Protects chafed skin associated with diaper rash and helps protect from wetness
  • Warnings

    When using this product avoid contact with eyes.  For external use only. 

    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 affected area, and allow to dry. Apply cream liberally as often as necessary, with each change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

  • Inactive ingredients

    BeesWax, Butyrospermum parkii (shea) butter, Carbopol, Cetylstearyl alcohol, Cholecalciferol (Vitamin D), Citric Acid, Ciclopentasiloxane, cyclotetrasiloxane, Dimethicone, Disodium EDTA, DMDM Hydantoin, Ethylhexyl palmitate, Glycerin, Glycina Soja (soybean)oil, Isopropyl palmitate, PEG-40 Castor Oil, Purified Water, Retinyl palmitate (Vitamin A), Sodium Hydroxide, Tocopherol(Vitamin E).




  • Akin Diaper Rash Cream 170 g

    Tube label

  • INGREDIENTS AND APPEARANCE
    AKIN DIAPER RASH 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    CYCLOMETHICONE 4 (UNII: CZ227117JE)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    PEG-40 CASTOR OIL (UNII: 4ERD2076EF)  
    WATER (UNII: 059QF0KO0R)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69822-003-06170 g in 1 TUBE; Type 0: Not a Combination Product04/25/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01604/25/2019
    Labeler - Southern Sales & Service, Inc. (013114906)
    Registrant - Southern Sales & Service, Inc. (013114906)
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