Label: YOU-V SPF-30 BROAD SPECTRUM SUNSCREEN- titanium dioxide, zinc oxide lotion
- NDC Code(s): 73243-045-03
- Packager: YouV, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Drug Facts
- Active ingredients
- Uses:
- Warnings:
-
Directions:
- Apply liberally 15 minutes before sun exposure and as needed.
- Children under 6 months of age: ask doctor
- Reapply at least every 2 hours.
- Reapply as needed or after towel drying, swimming, or sweating.
- Use a water-resistant sunscreen if swimming or sweating.
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including:
Sun Protection Measures:
- Limit time in the sun, especially between 10am and 2pm.
- Wear long-sleeved shirts, pants, hats, and sunglasses.
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Other ingredients:
Acrylates Copolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aluminum Hydroxide, Aqua (Deionized Water), Ascorbyl Palmitate (Vitamin C), Beeswax, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Carica Papaya Fruit Extract, Cetearyl Olivate, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil, Dimethicone, Ethyl Vanillin, Ethylhexylglycerin, Fluorescent Brightener 230, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Laminaria (Algae) Extract, Linoleic Acid, Norbornanediamine/ Resorcinol Diglycidyl Ether Crosspolymer, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, Rubus Idaeus (Raspberry) Extract, Sodium Hydroxide, Sorbitan Olivate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E).
- Other Information:
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
YOU-V SPF-30 BROAD SPECTRUM SUNSCREEN
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73243-045 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 35 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) WATER (UNII: 059QF0KO0R) ASCORBYL PALMITATE (UNII: QN83US2B0N) YELLOW WAX (UNII: 2ZA36H0S2V) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PAPAYA (UNII: KU94FIY6JB) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) COCONUT OIL (UNII: Q9L0O73W7L) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYL VANILLIN (UNII: YC9ST449YJ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) LINOLEIC ACID (UNII: 9KJL21T0QJ) GREEN OLIVE (UNII: 6HD2W46UEG) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) RASPBERRY (UNII: 4N14V5R27W) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN OLIVATE (UNII: MDL271E3GR) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73243-045-03 88 mL in 1 TUBE; Type 0: Not a Combination Product 07/22/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/22/2019 Labeler - YouV, LLC (117082836)