Label: DAILY SPF FACIAL SUNSCREENLOTION BROAD SPECTRUM SPF 32- zinc oxide cream
- NDC Code(s): 79356-201-10, 79356-201-20
- Packager: Onekind.25
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions:
Apply generously 15 minutes before sun exposer. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating.
Sun protection measures: Spending time in the sun increase 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 10am - 2pm.
- Wear long sleeved shirts, pants, hats and sunglasses.
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INACTIVE INGREDIENT
Inactive Ingredients: Water (Aqua), Caprylyc/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Tocopheryl Acetate, Helianthus annuus (sunflower) seed oil, Coco-Glucoside, Glyceryl Caprylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside , Xanthan Gum, Coco-Caprylate/Caprate, Lecithin, Caprylyl/Capryl Glucoside, Polyhydroxystearic Acid , Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Oryza Sativa Starch, Dipotassium Glycyrrhizate, Bisabolol, Caprylhydroxamic Acid, Sodium Pthalate, Sclerotium Gum, Sucrose, Phaeodactylum Tricornutum Extract, Glucose, Spirulina Maxima Extract, Tocopherol, C10 Alochol, C8 Alcohol.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY SPF FACIAL SUNSCREENLOTION BROAD SPECTRUM SPF 32
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79356-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 210 mg in 1 g Inactive Ingredients Ingredient Name Strength LEVOMENOL (UNII: 24WE03BX2T) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) PHYTATE SODIUM (UNII: 88496G1ERL) BETASIZOFIRAN (UNII: 2X51AD1X3T) SUCROSE (UNII: C151H8M554) PHAEODACTYLUM TRICORNUTUM (UNII: Y5W63E7HLV) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) SPIRULINA MAXIMA (UNII: 9K7IG15M0Q) TOCOPHEROL (UNII: R0ZB2556P8) C8-10 ALCOHOLS (UNII: 6X61I5U3A4) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) COCONUT ALKANES (UNII: 1E5KJY107T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARGAN OIL (UNII: 4V59G5UW9X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) COCO GLUCOSIDE (UNII: ICS790225B) SUNFLOWER OIL (UNII: 3W1JG795YI) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) SHEA BUTTER (UNII: K49155WL9Y) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) XANTHAN GUM (UNII: TTV12P4NEE) STARCH, RICE (UNII: 4DGK8B7I3S) ISOSTEARIC ACID (UNII: X33R8U0062) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79356-201-20 1 in 1 CARTON 11/03/2020 1 NDC:79356-201-10 48 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/03/2020 Labeler - Onekind.25 (080286020)
