Label: CORT ASTRIN- hydrocortisone solution

  • NDC Code(s): 50989-226-18, 50989-226-26
  • Packager: Vedco, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated November 15, 2022

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

View All Sections
  • PURPOSE

    FOR INFLAMMATORY PRURITUS

  • INDICATIONS:

    A topical treatment for the relief of inflammatory pruritic conditions in dogs.

    DOSAGE:

    Apply 3 to 4 times daily.

  • PRECAUTIONS:

    For topical use only. Not for opthalmic use. Not for deep seated infections.

  • KEEP OUT OF REACH OF CHILDREN

    For Animal Use Only


    For Topical Use Only


    Keep Out of Reach of Children

    image of EYE CLOCK

  • INGREDIENTS:

    Each mL contains:
    Burow’s Solution.........20 mg
    Hydrocortisone .. 10 mg

    In a water miscible propylene glycol base.

  • CONTRAINDICATIONS:

    As with any hydrocortisone product, Cort/Astrin Solution should not be used in the presence of tuberculosis of the skin. Store in a cool area.

  • Net Contents:

    1 oz (30 mL)

    16 oz (473 mL)

  •                                       1 oz (30 mL) Bottle/Case Label

    image of LBVETP103_r0909

  • 16 oz (473 mL)

    image OF LBVETP100_r0909

  • INGREDIENTS AND APPEARANCE
    CORT ASTRIN 
    hydrocortisone solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50989-226
    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:50989-226-1812 in 1 CASE
    130 mL in 1 BOTTLE, DROPPER
    2NDC:50989-226-2612 in 1 CASE
    2473 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/07/2009
    Labeler - Vedco, Inc. (021634266)
    Establishment
    NameAddressID/FEIBusiness Operations
    FIRST PRIORITY INCORPORATED179925722manufacture, label
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

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