SKIN SO SOFT BUG GUARD PLUSITCH RELIEF ITCH RELIEF- menthol spray

skin so soft bug guard plusitch relief by

Drug Labeling and Warnings

skin so soft bug guard plusitch relief by is a Otc medication manufactured, distributed, or labeled by Avon Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Menthol 0.5 %......

       Purpose
.........External Analgesic

INDICATIONS & USAGE

Uses
For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

WARNINGS

Warnings
For external use only

When using this product

• Avoid contact with eyes. If contact occurs, rinse with water to remove

Stop use and ask a doctor if

• If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions
Adults and children 2 years of age and older:

• Apply to affected area not more than 3 to 4 times daily
  

Children under 2 years of age:

• Consult a doctor before use

INACTIVE INGREDIENT

Inactive Ingredients:
Water/Eau, C12-15 Alkyl Benzoate, Ethylhexyl Palmitate, Glycerin, SD Alcohol 40-B, Butylene Glycol, Glyceryl Stearate, Ceteareth-20,Avena Sativa (Oat) Meal Extract, Citric Acid, Ceteareth-12, Cetearyl Alcohol, Cetyl Palmitate, Cholesterol, Chlorphenesin, Sodium Hydroxide, Sodium Dehydroacetate.

QUESTIONS

Questions?
Call 1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKIN SO SOFT BUG GUARD PLUSITCH RELIEF   ITCH RELIEF
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0282
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A)	Menthol	5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0282-1	59 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/18/2012

Labeler - Avon Products, Inc. (001468693)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Products, Inc.		005149471	manufacture(10096-0282)