Skin So Soft Bug Guard Plus IR3535 description, usages, side effects, indications, overdosage, supplying and lots more!

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Skin So Soft Bug Guard Plus IR3535

Avon Products, Inc




FULL PRESCRIBING INFORMATION

Uses

Helps prevent sunburn

DIRECTIONS FOR USE: It is a violation of Federal law to use this product in a manner inconsistent with its labeling. Apply liberally 15 minutes before sun and insect exposure. An adult must apply this product to children under 10. Children under 6 months: Ask a doctor. For insect protection, reapply about every 2 hours or sooner if effectiveness diminishes. For sunscreen protection, reapply immediately after towel drying, after 80 minutes of swimming, or sweating, at least every 2 hours. Do not exceed 9 applications per day.

STORAGE: Store in cool, dry place away from heat or flame.

Protect this product from sun.

Caution. For external use only. Causes moderate eye irritation. When using this product keep out of eyes. Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs. Keep out of reach of children. Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early aging. This product has been shown only to prevent sunburn, not skin cancer or early aging.

Active ingredient

ACTIVE SUNSCREEN INGREDIENTS: Octinoxate 7.5%, Oxybenzone 6%, Octisalate 5%

OTHER INGREDIENTS: Water, Butylene Glycol, Glycerin, PVP/Eicosene Copolymer, Aloe Barbadensis Gel, Isostearic Acid, Propylene Glycol Myristyl Ether Acetate, Stearic Acid, Benzyl Alcohol, Cetyl Alcohol, DEA-Oleth-3 Phosphate, Diglycol/CHDM/Isophthalates/SIP Copolymer, Dimethicone, Glyceryl Stearate, Magnesium Aluminum Silicate, Tocopheryl Acetate, Barium Sulfate, Fragrance, Imidazolidinyl Urea, Xanthan Gum, Disodium EDTA, Blue 1, Red 33.

Skin So Soft Bug Guard Plus IR3535 Skin So Soft Bug Guard Plus IR3535

Skin So Soft Bug Guard Plus IR3535

Octinoxate, Oxybenzone, Octisalate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10096-0071
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
OXYBENZONE OXYBENZONE 60 mg
OCTISALATE OCTISALATE 50 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10096-0071-1 118 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-02-12


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