Label: DERMABLISS ANTI-ITCH AND ALLERGY RELIEF- hydrocortisone, pramoxine hydrochloride spray
- NDC Code(s): 80547-101-04, 80547-101-08
- Packager: Vetnique Labs 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 October 5, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- PRODUCT FACTS
- Active Ingredients
- Ingredients:
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DIRECTIONS
Use on dry skin. Spray directly on affected anal area and massage liquid into skin until absorbed. Wash hands after use. Use no more than 4 times a day, or as directed by a veterinarian.
FOR BEST RESULTS Use with our Furbliss® pet brushes, soothing Dermabliss™ Anti-Itch & Allergy Relief Shampoo, and full line of Dermabliss™ products for seasonal allergy relief.
- CAUTION
- WARNING
- STORAGE
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SPL UNCLASSIFIED SECTION
VETERINARIAN RECOMMENDED
SOOTHING OATMEAL
MEDICATED CLINICAL STRENGTH
ditch the itch!™
RELIEVES ITCHING
REDUCES INFLAMMATION
MOISTURIZING FORMULA
SOOTHING & HYDRATING
FOR DOGS & CATS
Vet founded. Vet formulated.
Vet recommended.™Made in the USA from US & Global Ingredients
Distributed by Vetnique Labs®
US: 1748 W. Jefferson Ave #160, Naperville, IL 60540
UK: 1st Floor Cobham MSA, M25, Junction 9/10 Cobham KT11 3DB
Questions? 800-643-7558 • www.vetnique.com
V+ Created by Vets for Happy Pets™
- Packaging
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INGREDIENTS AND APPEARANCE
DERMABLISS ANTI-ITCH AND ALLERGY RELIEF
hydrocortisone, pramoxine hydrochloride sprayProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:80547-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10 mg in 1 mL PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:80547-101-04 118 mL in 1 BOTTLE 2 NDC:80547-101-08 237 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/12/2020 Labeler - Vetnique Labs Llc (945367014)