Label: DOCTOR OS DIAPER BALM- zinc oxide ointment

  • NDC Code(s): 73570-001-02
  • Packager: Dr. O's Dermabalm, Llc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 8, 2021

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active ingredients

    Zinc Oxide 30%

  • Purpose

    Skin protectant

  • Uses

    • Helps treat and prevent diaper rash
    • Protects minor skin irritation associated with diaper rash and helps seal out wetness
  • Warnings

    For external use only.

    When using this product • Keep out of 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 the reach of children. If swallowed seek medical attention or contact a Poison Control Center right away.

  • Directions

    • change wet and soiled diapers promptly
    • cleanse the diaper area and allow to dry
    • apply ointment liberally as often as necessary with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged
  • Other information

    Store between 15 and 30°C (59 and 86°F).

  • Inactive ingredients

    Lanolin, corn starch, soy lecithin, sesame seed oil, fragrance

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    DOCTOR OS DIAPER BALM 
    zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73570-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION30 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    SESAME OIL (UNII: QX10HYY4QV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73570-001-021 in 1 CARTON02/14/2020
    1100 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34702/14/2020
    Labeler - Dr. O's Dermabalm, Llc (016334106)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL TECHNOLOGY, LLC618561906manufacture(73570-001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!