Moisture Therapy description, usages, side effects, indications, overdosage, supplying and lots more!

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Moisture Therapy

Avon Products, Inc.




FULL PRESCRIBING INFORMATION

Active ingredient

​Active Ingredients

​Octinoxate, 7.5%..........

Octisalate, 5.0%..........

Oxybenzone, 1.0%............

Purpose

​Purpose

​........Sunscreen

........Sunscreen

........Sunscreen

Uses

Uses
• helps prevent sunburn

Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

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

Directions
• apply generously and evenly 15 minutes before sun exposure
• children under 6 months of age: ask a doctor
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating

Other Information
• protect the product in this container from excessive heat and direct sun.

Inactive ingredients: WATER/EAU, GLYCERIN, BUTYLENE GLYCOL, GLYCERYL STEARATE, PEG-8, SILICA, ORYZA SATIVA (RICE) BRAN OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, HYDROGENATED POLYISOBUTENE, LECITHIN, HYDROGENATED LECITHIN, GLYCINE SOJA (SOYBEAN) STEROLS, GLYCINE SOJA (SOYBEAN) OIL, CETYL ALCOHOL, DIMETHICONE, CARBOMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, POLYGLYCERYL-3 DIISOSTEARATE, DISODIUM EDTA, IMIDAZOLIDINYL UREA, DIMETHICONOL, METHYLPARABEN, SODIUM HYDROXIDE, PARFUM/FRAGRANCE.

Questions or comments? Call 1-800-FOR-AVON or 1-800-265-AVON in Canada.

Moisture Therapy Moisture Therapy Moisture Therapy

Moisture Therapy

OCTINOXATE, OCTISALATE, OXYBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10096-0249
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
OCTISALATE OCTISALATE 50 mg
OXYBENZONE OXYBENZONE 10 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10096-0249-1 400 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-04-11


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