Label: BLACK AND WHITE SKIN PROTECTANT- petrolatum ointment

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

Drug Label Information

Updated October 21, 2023

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  • Active Ingredients:

    Petrolatum, 62%

    Purpose

    Skin Protectant

  • Uses:

    Temporarily protects minor

    • cuts
    • scrapes
    • burns
    • chapped or cracked skin
  • Warnings:

    For External Use Only.

    Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

    • do not get into eyes

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last for 7 days or clear up and occur again within a few days

    Keep out of reach of children.

    • If swallowed, get medical help or call a poison control center at once.
  • Directions:

    • Apply as needed.
  • Other Ingredients:

    Beta Carotene, D&C Green 6, D&C Red 17, Glycerin, Hydrogenated Vegetable Oil, Lanolin, Microcrystalline Wax, Ozokerite, Resorcinol, Synthetic Bees-wax, Turpentine.

  • Package Labeling

    12022-004-00

  • INGREDIENTS AND APPEARANCE
    BLACK AND WHITE SKIN PROTECTANT 
    petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM620 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    .BETA.-CAROTENE (UNII: 01YAE03M7J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LANOLIN (UNII: 7EV65EAW6H)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    CERESIN (UNII: Q1LS2UJO3A)  
    RESORCINOL (UNII: YUL4LO94HK)  
    TURPENTINE (UNII: XJ6RUH0O4G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-004-001 in 1 CARTON12/01/1990
    164 g in 1 CAN; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/01/1990
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-004)
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