Label: CHEW PLUS HEAL ADVANCED HYDROCORTISONE- hydrocortisone, pramoxine hydrochloride spray

  • NDC Code(s): 86173-886-04, 86173-886-08
  • Packager: Click Industries LLC
  • 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 March 11, 2025

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

View All Sections
  • Product Facts

  • Active Ingredients:

    Hydrocortisone................................ 1%
    Pramoxine Hydrochloride............... 0.5%

  • Inactive Ingredients: 

    Propylene Glycol, Water, Ethyl Alcohol, Glycerin, PEG-75 Lanolin, Hydrolyzed Oats, Benzyl Alcohol.

  • DIRECTIONS FOR USE

    Spray directly on affected areas and massage liquid into skin until absorbed. Wash hands after use. Use no more than 3 times a day, or as directed by a veterinarian.

  • Cautions:

    For animal use only. Do not allow animal to lick affected areas. If irritation persists or worsens, discontinue use and contact a veterinarian. Do not use on puncture wounds, burns, or lacerations.

  • Warnings: 

    Keep out of reach of children. Avoid contact with eyes. If eye contact occurs, rinse thoroughly with water and consult a veterinarian.

  • Storage:

    Store at room temperature. Protect from freezing.

  • SPL UNCLASSIFIED SECTION

    ✓ MEDICATED SPRAY

    ✓ SKIN IRRITATIONS

    ✓ INFLAMMATION

    ✓ MOIST ECZEMA

    FOR DOGS

    Manufactured For:
    Chew + Heal
    Surfside, FL
    www.chewandheal.com
    MADE IN U.S.A.
    with globally sourced ingredients 

  • Packaging

    ADVANCED HYDROCORTISONE

  • INGREDIENTS AND APPEARANCE
    CHEW PLUS HEAL ADVANCED HYDROCORTISONE 
    hydrocortisone, pramoxine hydrochloride spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86173-886
    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)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86173-886-04118 mL in 1 BOTTLE, SPRAY
    2NDC:86173-886-08237 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/21/2025
    Labeler - Click Industries LLC (117033580)
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!