Dermal-Soothe description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Dermal-Soothe

Vetoquinol USA, Inc.

Micro Pearls Advantage Dermal-Soothe™ Spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Patented Continuous
Moisture Release

INDICATIONS

A soothing, anti-itch, moisturizing spray for application after shampooing or between shampoos as needed. Aids in the relief of itching and flaking due to dry skin. May be used with other medicated shampoos as directed by your veterinarian.

DERMAL-SOOTHE DESCRIPTION

Micro Pearls® Advantage Dermal-Soothe™ Anti-Itch Spray is a remarkable breakthrough in animal care technology. Dermal-Soothe™ Anti-Itch Spray contains itch-relieving Pramoxine Hydrochloride and Novasome® microvesicles designed to deliver long-lasting moisture factors to the hair and epidermal layers in a humidifying spray containing Lactamide MEA. The result is an itch relieving spray that leaves your pet with a coat that is soft, supple and lustrous.

DIRECTIONS

Shake well. Spray liberally onto damp or dry coat, allowing spray to reach the skin. Repeat as necessary.

INGREDIENTS

1% Pramoxine Hydrochloride in a base containing Lactamide MEA (a Lactic Acid derivative emolient) and Novasome® microvesicles.

PRECAUTIONS

For topical use only on dogs and cats. Avoid contact with eyes and mucous membranes. Discontinue use if skin becomes irritated or inflamed.

AVAILABLE ONLY THROUGH LICENSED VETERINARIANS. KEEP OUT OF REACH OF CHILDREN. FOR ANIMAL USE ONLY.

Novasome® is a registered
trademark of Micro Pak, Inc.

Manufactured for:
Vétoquinol USA, Inc.
Ft. Worth, TX (USA) 76137
www.vetoquinolusa.com

411528
Lot
6
Exp. Date

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label

Micro Pearls® Advantage

Dermal-Soothe™
Spray

ANTI-ITCH
SPRAY FOR
DOGS & CATS

Patented Novasome®
Microvesicles
for Continuous
Moisture Release

Net Wt. 12 fl oz (355 mL)

Vétoquinol

Dermal-Soothe

Dermal-Soothe

Pramoxine Hydrochloride SPRAY

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:17030-041
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
pramoxine hydrochloride PRAMOXINE 10 mg

Inactive Ingredients

Ingredient Name Strength
water
CITRIC ACID MONOHYDRATE
N-Lactoyl Ethanolamine
quaternium-15

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:17030-041-12 355 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1999-12-29


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.