Label: KOVR ALL-NATURAL SPF-30 MOISTURIZING SUNSCREEN FOR WOMEN- titanium dioxide, zinc oxide cream
- NDC Code(s): 83531-499-00
- Packager: ACTIVE LIFE INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses:
- WARNINGS:
-
Directions:
Apply liberally and evenly prior to sun exposure. Reapply after towel drying, or prolonged swimming or sweating. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including limiting time in the sun, especially between 10 a.m. - 2 p.m., and wearing long-sleeve shirts, pants, hats and sunglasses. For use on children under 6: consult a physician.
Sun Protection Measures: - Other Information:
-
Inactive Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Camellia Sinensis (Green Tea) Extract, Daucus Carota Sativa (Carrot) Extract, Ethylhexylglycerin, Ethylhexyl Palmitate, Glycerin, Glycine Soja (Soybean) Oil, Helianthus Annuus (Sunflower) Oil, Lecithin, Phenoxyethanol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sesamum Indicum (Sesame) Seed Oil, Sodium Laurylglucosides Hydroxypropylsulfonate, Theobroma Cocao (Cocoa) Butter, Tocopherol (Vitamin E), Xanthan Gum.
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
KOVR ALL-NATURAL SPF-30 MOISTURIZING SUNSCREEN FOR WOMEN
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83531-499 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 60 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CARROT (UNII: L56Z1JK48B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYLHEXYL PALMITATE (UNII: 2865993309) GLYCERIN (UNII: PDC6A3C0OX) SOYBEAN OIL (UNII: 241ATL177A) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALMOND OIL (UNII: 66YXD4DKO9) SESAME OIL (UNII: QX10HYY4QV) SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: Z6GFR7R72Y) COCOA (UNII: D9108TZ9KG) TOCOPHEROL (UNII: R0ZB2556P8) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83531-499-00 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/19/2023 Labeler - ACTIVE LIFE INC (087241186)
