SUN Solar Defense Hydrating description, usages, side effects, indications, overdosage, supplying and lots more!

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SUN Solar Defense Hydrating

Allure Labs, Inc.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients:

Zinc Oxide 5%

Ethylhexyl Methoxycinnamate (Octinoxate) 7.5%

Benzophenone-3 3%

Ethylhexyl Salicylate (Octisalate) 5%

Uses

Uses:

A hydrating 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

Directions:

Apply to cleaned skin every morning for ultimate protection.

Indications: Dry, dehydrated, rosacea, sensitive.

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 Ingredients:

Deionized water (Aqua), C12-15 Alkyl Benzoate, Glyceryl Stearate (and) PEG-100 Stearate, Glycerin, Sodium Hyaluronate, Imperata Cylindrica Root Extract, Octyl Dodecyl Neopentanoate, Sorbitol, Caprylic/Capric Truglyceride, Camellia sinensis (Green Tea) Leaf Extract, Biosaccharide Gum-1, Algae Extract and Mugwort Extract, Caprylyl Glycol and Phnoxyethanol and Hexylene Glycol, Sodium PCA, Lecithin, Sorbitan Stearate, Symphytum Officinale Extract and Plantago Ovata Seed Extract, Yeast Extract, Aloe Barbadensis Leaf Extract, Spiraea Ulmaria Flower Extract (and) Centella Asiatica Extract, Magnesium Aluminum Silicate, Tocopheryl Acetate, Ascorbyl Palmitate, Disodium EDTA, Dipotassium Glycyrrizate, Amino Acids.

Image of the Product:

SUN Solar Defense Hydrating

Distributor:

Image International

Palm Beach, FL 33411 USA

www.imageskincare.com

SUN Solar Defense Hydrating

Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62742-4037
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 50 mg
OCTINOXATE OCTINOXATE 75 mg
OXYBENZONE OXYBENZONE 30 mg
OCTISALATE OCTISALATE 50 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62742-4037-1 118 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-01-01


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