A AND D (PETROLATUM) OINTMENT [H&H LABORATORIES, INC.]

A AND D (PETROLATUM) OINTMENT [H&H LABORATORIES, INC.]
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NDC 52471-101-05, 52471-101-47
Set ID 00bc354f-9f7b-4288-9bbe-a140a6643d20
Category HUMAN OTC DRUG LABEL
Packager H&H Laboratories, Inc.
Generic Name
Product Class
Product Number
Application Number PART347
  • ACTIVE INGREDIENT

    Active Ingredient (in each gram): White Petrolatum 93.5%

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  • PURPOSE

    Purpose-Skin Protectant

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  • INDICATIONS & USAGE

    Uses-Temporarily protects minor cuts, scrapes, and sunburn.     Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

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  • DOSAGE & ADMINISTRATION

    Directions: Apply liberally as needed  Change wet and soiled diapers promptly.  Cleanse the diaper area and allow to dry. Use with each diaper change, especially at bedtime when exposure to wet diapers may be prolonged.

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  • KEEP OUT OF REACH OF CHILDREN

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

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  • WARNINGS

    For external use only.  Avoid contact with eyes.  on deep puncture wounds, animal bites, or serious burns.

    Stop use and ask a doctor if condition worsens, symptoms last for more than 7 days or clear up and occur again within a few days.

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D

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  • PRINCIPAL DISPLAY PANEL

    MM1



    H and H AD Carton.jpg






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  • INGREDIENTS AND APPEARANCE
    A AND D 
    petrolatum ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52471-101
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 937.5 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ERGOCALCIFEROL (UNII: VS041H42XC)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52471-101-47 144 in 1 CARTON
    1 NDC:52471-101-05 5 g in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 05/14/2012
    Labeler - H&H Laboratories, Inc. (151357175)
    Registrant - H&H Laboratories, Inc. (151357175)
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