NDC | 70068-001-01 |
Set ID | 1fa57891-1800-4192-ad7e-bc48f27ad185 |
Category | HUMAN OTC DRUG LABEL |
Packager | IDLife, LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
For sunscreen use:
- Apply liberally 15 minutes before sun exposure.
- Use a water resistant sunscreen if swimming or sweating.
- Reapply at least every two hours.
- Children under 6 months: Ask a doctor.
- Sun Protection Measures. 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:
•Limit time in the sun, especially from 10 a.m.–2 p.m.
•Wear long-sleeved shirts, pants, hats, and sunglasses. - Other Information
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Inactive Ingredients
Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetearyl Glucoside, Cetyl Esters, Cichorium Intybus (Chicory) Root Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Coco-Caprylate /Caprate, Dimethicone, Dipotassium Glycyrrhizinate, Ethylhexylglycerin, Ethyl Linoleate, Glycerin, Glyceryl Stearate SE, Hydrolyzed Soybean Fiber, lsopropyl Palmitate, Kappaphycus Alvarezii Extract, Lens Esculenta (Lentil) Fruit Extract, Panthenol, Phenoxyethanol, Pyrus Malus (Apple)Fruit Extract, Sclerotium Gum, Shorea Stenoptera Seed Butter, Sodium Lactate, Sodium PCA, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Tropaeolum Majus Flower/Leaf/Stem Extract, Xanthan Gum
- Questions?
- Product Label
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INGREDIENTS AND APPEARANCE
DAY DAILY ANTI-AGING MOISTURIZING FACE BROAD SPECTRUM SPF 20 SUNSCREEN
zinc oxide, octinoxate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70068-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 50 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) SHEANUT OIL (UNII: O88E196QRF) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETYL ESTERS WAX (UNII: D072FFP9GU) CHICORY ROOT (UNII: 090CTY533N) COCO-CAPRYLATE (UNII: 4828G836N6) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYL LINOLEATE (UNII: MJ2YTT4J8M) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) KAPPAPHYCUS ALVAREZII (UNII: T479H08K2O) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) BETASIZOFIRAN (UNII: 2X51AD1X3T) SHOREA STENOPTERA SEED BUTTER (UNII: 129R0X862G) SODIUM LACTATE (UNII: TU7HW0W0QT) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROPAEOLUM MAJUS FLOWERING TOP (UNII: RGT30824HY) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70068-001-01 1 in 1 BOX 08/26/2015 1 44.5 mL in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/26/2015 Labeler - IDLife, LLC (051244896)