- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
-
Uses
- Helps prevent sunburn.
- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure. Works best on moisturized skin.
- Reapply:
- After 40 minutes of swimming or sweating.
- Immediately after towel drying.
- At least every 2 hours.
- Children under 6 months: ask a doctor.
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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 value 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.
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Inactive ingredients
Cyclopentasiloxane, Caprylic/Capric Triglyceride, Dimethicone Crosspolymer, Glycerin, Water, Dimethicone/Vinyl Dimethicone Crosspolymer, Spirulina Maxima Extract, Camellia Sinensis Leaf Extract, Opuntia Ficus-Indica Stem Extract, Palmaria Palmata Extract, Disodium Lauriminodipropionate Tocopheryl Phosphates, Citrus Paradisi (Grapefruit) Seed Extract, Ascorbic Acid, Dimethiconol, Vanilla Planifolia Fruit Extract, Fusanus Spicatus Wood Oil, Dimethicone, Triethoxycaprylylsilane, Benzoic Acid, Dehydroacetic Acid, Phenoxyethanol, Farnesol, Iron Oxides (CI 77491, CI 77492, CI 77499)
- Other information
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton
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INGREDIENTS AND APPEARANCE
DAILY UV PROTECTOR SPF 30 SUNSCREEN
titanium dioxide and zinc oxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68078-019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide 54 mg in 1 mL Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 54 mg in 1 mL Inactive Ingredients Ingredient Name Strength Cyclomethicone 5 (UNII: 0THT5PCI0R) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Dimethicone Crosspolymer (450000 MPA.S AT 12% IN Cyclopentasiloxane) (UNII: UF7620L1W6) Glycerin (UNII: PDC6A3C0OX) Water (UNII: 059QF0KO0R) Dimethicone/Vinyl Dimethicone Crosspolymer (Soft Particle) (UNII: 9E4CO0W6C5) Arthrospira Maxima (UNII: 9K7IG15M0Q) Green Tea Leaf (UNII: W2ZU1RY8B0) Opuntia Ficus-Indica Stem (UNII: MUD8892KHL) PALMARIA PALMATA (UNII: 7832HOY4ZQ) Disodium Lauriminodipropionate Tocopheryl Phosphates (UNII: 0K5Y9U1P6M) Citrus Paradisi Seed (UNII: 12F08874Y7) Ascorbic Acid (UNII: PQ6CK8PD0R) Dimethiconol (100000 CST) (UNII: OSA9UP217S) VANILLA BEAN (UNII: Q74T35078H) Santalum Spicatum Oil (UNII: H9LVS6REV4) Dimethicone (UNII: 92RU3N3Y1O) Triethoxycaprylylsilane (UNII: LDC331P08E) Benzoic Acid (UNII: 8SKN0B0MIM) Dehydroacetic Acid (UNII: 2KAG279R6R) Phenoxyethanol (UNII: HIE492ZZ3T) Farnesol (UNII: EB41QIU6JL) Ferric Oxide Yellow (UNII: EX438O2MRT) Ferric Oxide Red (UNII: 1K09F3G675) Ferrosoferric Oxide (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68078-019-20 1 in 1 CARTON 02/01/2017 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:68078-019-02 1 mL in 1 PACKET; Type 0: Not a Combination Product 02/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 02/01/2017 Labeler - Colorescience (128731929)