Label: PET MD HYDROCORTISONE 1% PLUS- hydrocortisone, pramoxine hydrochloride spray

  • 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 August 31, 2023

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  • Active Ingredients:

    Hydrocortisone 1%,
    Pramoxine Hydrochloride 0.5%.

  • INDICATIONS & USAGE

    Pet MD Hydrocortisone 1% PLUS helps to relieve symptoms of hot spots, bites and skin conditions so your pet can heal quickly.

  • Inactive Ingredients:

    Propylene Glycol, Water, SD Alcohol 40B, Glycerin, PEG-75 Lanolin, Hydrolyzed Oats, Benzyl Alcohol.

  • Directions for Use:

    Spray directly onto the affected area(s) up to 3 times daily, or as directed by veterinarian. Do not allow animal to lick the treated areas until dry to prevent ingestion.

  • Precautions:

    Avoid contact with eyes or mucous membranes. If eye contact occurs, rinse thoroughly with water and consult a veterinarian. 

  • Cautions:

    If undue skin irritation develops or increases, discontinue use and consult a veterinarian.

  • Storage:

    Store at controlled room temperature. 

  • SPL UNCLASSIFIED SECTION

    formulated for dogs & cats

    ADVANCED FORMULATION

    Manufactured for:
    Pet MD Brands, LLC
    Odessa, FL 33556
    PetMDStore.com

    MADE IN THE USA

  • Packaging

    PetMD-016

  • INGREDIENTS AND APPEARANCE
    PET MD HYDROCORTISONE 1% PLUS 
    hydrocortisone, pramoxine hydrochloride spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86090-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 mL
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    OAT (UNII: Z6J799EAJK)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86090-016-04118 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/31/2023
    Labeler - Pet MD Brands, LLC (060164988)
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