Label: DERMAQUEST SKIN THERAPY DAILY MOISTURIZING SPF 15- zinc oxide lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 62742-4053-1, 62742-4053-2 - Packager: Allure Labs, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 26, 2010
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- Official Label (Printer Friendly)
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INDICATIONS & USAGE
Optimal for daily use, this state-of-the-art lotion contains Zinc Oxide to help protect against the damaging effects of UVA and UVB rays. Cosmetically elegant and hydrating, this lotion id ideal for sensitive skin and post professional treatments.
DIRECTIONS:
Apply daily to the fingertips and gently massage into the skin. Reapply as needed. Discontinue use if irritation develops.
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
Water (Aqua), Cyclomethicone, Glycerin, Glyceryl Stearate (and) PEG-100 Stearate, Sorbitol, Imperata Cyclidrica (Root) Extract, Caprylyl Glycol, Sorbitan Stearate, Lecithin, Arabidopsis Extract, Plakton Extract, Xanthan Gum, Carbomer, Ascorbyl Palmitate (Vitamin C), Tocopheryl Acetate (Vitamin E), Citric Acid, Disodium EDTA.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMAQUEST SKIN THERAPY DAILY MOISTURIZING SPF 15
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 95 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4053-1 29.6 mL in 1 TUBE 2 NDC:62742-4053-2 59.2 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)
