SUN SOLAR DEFENSE ORGANIC SPF30- zinc oxide cream

SUN Solar Defense Organic SPF30 by

Drug Labeling and Warnings

SUN Solar Defense Organic SPF30 by is a Otc medication manufactured, distributed, or labeled by Allure Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Zinc Oxide

PURPOSE

Purpose:

Sunscreen

INDICATIONS & USAGE

Uses:

• An organic UVA/UVB broad spectrum daily moisturizer. Provides ultimate protection against the aging effects of the sun and other environmental exposures. Enriched with essential vitamins and anti-oxidants that prevent free radical damage and preserving skin hydration for the entire day.

• Water Resistant
• Paraben Free

• Chemical free

Directions:

Apply liberally 15-30minute prior to sun exposure. Reapply after prolonged swimming or vigorous activity.

Indications:

Sensitive skin highly exposed to sun

WARNINGS

Warnings:

For external use only

When using this product

• Keep out of eyes. If contact occurs rinse with water.
• Discontinue use if irritation or redness occurs

Keep out of reach of children

INACTIVE INGREDIENT

Inactive Ingredients:

Water (Aqua), Cyclomethicone, Glycrin, Glyceryl Stearate (and) PEG 100 Stearate, Sorbitol, Imperata Cylindrica Root Extract, Polyacrylamide and C13-14 Isoparaffin and Laureth-7, Caprylyl Glycol and Phenoxyethanol and Hexylene Glycol, Lecithin, Ascorbyl Palmitate (Vitramin C), Xanthan Gum, Dipotassium Glyrhhizate, Olea Europea (Olive) Leaf Extract, Disodium EDTA.

PRINCIPAL DISPLAY PANEL

Distributor:

Image International

Palm Beach, FL 33411 USA

www.imageskincare.com

Image of the product:

INGREDIENTS AND APPEARANCE

SUN SOLAR DEFENSE ORGANIC SPF30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	190 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4038-1	118 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	01/01/2010

Labeler - Allure Labs, Inc. (926831603)