Label: CORTI DERM- hydrocortisone solution

  • NDC Code(s): 58829-160-10
  • Packager: FIRST PRIORITY INCORPORATED
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Updated November 15, 2022

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  • INFORMATION FOR OWNERS/CAREGIVERS

    Topical Treatment For the Relief of Discomfort Caused by Inflammatory Pruritus In Dogs

    For Animal Use Only • Keep Out of Reach of Children

  • HYDROCORTISONE:

    − Anti-inflammatory

    − Anti-pruritic

  • BURROW'S SOLUTION:

    − Astringent for drying of moist dermatitis.

    − Provides cooling for relief of discomfort.

  • CONTRAINDICATION:

    As with any topical hydrocortisone product Cort-Derm™ should not be used in the presence of tuberculosis of the skin.

    image of eye clock

  • INGREDIENTS:

    Hydrocortisone........................... 10 mg

    Burow's Solution......................... 20 mg

  • INACTIVE INGREDIENT

    In a water miscible base containing Propylene Glycol.

  • DOSAGE:

    Apply 3 to 4 times daily.

  • PRECAUTIONS:

    For topical use only.  Not intented for deep-seated infections.  Not for use in the eyes.

  • Net Contents:

    1 oz (30 mL) Reorder No. TP100PC

    4 oz (120 mL) Reorder No. TP102PC

    NOT RETURNABLE IF OUTDATED

    Made in U.S.A.

    Manufactured By: First Priority, Inc., Elgin, IL U.S.A.

    www.prioritycare.com

  •                                       1 oz (30 mL) Bottle/Case Label

    image of 1 oz (30 mL) bottle/case label

    Rev. 03-07

  • INGREDIENTS AND APPEARANCE
    CORTI DERM 
    hydrocortisone solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:58829-160
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10.2 mg  in 1 mL
    ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE.73 mg  in 1 mL
    ACETIC ACID (UNII: Q40Q9N063P) (ACETIC ACID - UNII:Q40Q9N063P) ACETIC ACID0.624 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58829-160-1012 in 1 CASE
    130 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/01/2009
    Labeler - FIRST PRIORITY INCORPORATED (179925722)
    Establishment
    NameAddressID/FEIBusiness Operations
    FIRST PRIORITY INCORPORATED179925722manufacture
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