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Zinc Oxide (H&H Laboratories, Inc.)

Available Formats

Dosage Form Package Information Links
OINTMENT 1 TUBE in 1 CARTON (52471-116-48) > 28 g in 1 TUBE (52471-116-01) Label Information
OINTMENT 454 g in 1 JAR (52471-116-16) Label Information

Complete Zinc Oxide Information

  • ACTIVE INGREDIENT

    Active Ingredients Zinc oxide 20%


  • PURPOSE

    Purpose: Skin Protectant


  • INDICATIONS & USAGE

    Dries the oozing and weeping of poison ivy, poison oak, and sumac.  Helps treat/prevent diaper rash. Protects chafed skin associated with diaper rash and helps protect from wetness.


  • WARNINGS


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

    Stop use and ask a doctor if condition worsens or does not improve in 7 days



  • DOSAGE & ADMINISTRATION

    Directions:  Apply liberally as often as necessary.  For diaper rash: Change wet and soiled diapers promptly.  Cleanse the diaper area and allow to dry.  Apply liberally as often as necessary with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

  • INACTIVE INGREDIENT

    Inactive Ingredient:  White Petrolatum


  • PRINCIPAL DISPLAY PANEL

    16 ounce jar

    MM1


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center immediately.


  • INGREDIENTS AND APPEARANCE
    ZINC OXIDE 
    zinc oxide ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52471-116
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 200 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52471-116-48 1 in 1 CARTON
    1 NDC:52471-116-01 28 g in 1 TUBE
    2 NDC:52471-116-16 454 g in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part347 05/03/2012
    Labeler - H&H Laboratories, Inc. (151357175)
    Registrant - H&H Laboratories, Inc. (151357175)
    Establishment
    Name Address ID/FEI Business Operations
    Ultra Seal Corporation 085752004 manufacture