Label: EARLY MOMMY BABY BUM BUTTA- zinc oxide ointment

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

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredient

    Zinc Oxide 14%

    Purpose

    Skin protectant

  • Uses

    • Temporarily protects minor:
    • cuts
    • scrapes
    • burns
    • Temporarily protects chapped or cracked skin.
    • Dries the oozing and weeping of poison:
    • ivy
    • oak
    • sumac
  • Warnings

    For external use only

    Do not use on

    • deep or puncture wound
    • animal bites
    • serious burns

    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.

    If pregnant or breast-feeding,

    ask a health professional before use

  • Directions

    • apply as needed
  • Inactive ingredients:

    Beeswax, Cholecalciferol (Vitamin D3), Glycerin, Lanolin, Oat Protein, Petrolatum, Retinyl Palmitate (Vitamin A), Zea Mays (Corn) Starch

  • Other information:

    • Protect the product in this container from excessive heat and direct sun.

  • Questions?

    1-732-852-2596

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    EARLY MOMMY BABY BUM BUTTA 
    zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81638-171
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION140 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81638-171-00118 mL in 1 JAR; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/01/2021
    Labeler - TEKT TONE LABS LLC (044494980)
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