Label: DERMAQUEST SKIN THERAPY POST-SKIN RESURFACING BALM- hydrocortisone cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 August 19, 2010

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT:

    Hydrocortisone 1%

  • PURPOSE

    PURPOSE:

    Anti-itch

  • INDICATIONS & USAGE

    USES:

    • promotes healing of itchy skin
    • keeps skin hydrated


  • WARNINGS

    WARNINGS:

    For external use only.

    Ask a doctor if bleeding occurs or conditions worsens


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of chilren.

    If swallowed get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS:

    Apply to the skin as instructed by your skincare professional to keep the skin hydrated and to promote healing.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:

    Petrolatum, Tocopheryl Acetate (Vitamin E), Carthamus Tinctorius (Safflower) Seed Oil, Ubiquinone (Co-Enzyme Q10), Zinc Oxide (Cl 77947), Titanium Dioxide (Cl 77891), Ascorbyl Palmiate (Vitamin C), Glycosaminoglycans.

  • PRINCIPAL DISPLAY PANEL

    DISTRIBUTOR:

    DermaQuest, Inc.

    Hayward, CA

    dermaquestinc.com


    IMAGE OF PRINCIPAL DISPLAY PANEL:

    Principal Display Panel: Post-Skin Resurfacing Balm



  • INGREDIENTS AND APPEARANCE
    DERMAQUEST SKIN THERAPY POST-SKIN RESURFACING BALM 
    hydrocortisone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4051-159.2 mL in 1 TUBE
    2NDC:62742-4051-2236.6 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/01/2010
    Labeler - Allure Labs, Inc. (926831603)
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