Label: SUNFORGETTABLE TOTAL PROTECTION SHEET MATTE SUNSCREEN SPF 30- zinc oxide powder
- NDC Code(s): 68078-036-01
- Packager: Colorescience
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
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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.
- Reapply at least every 2 hours.
- Use a water resistant sunscreen if swimming or sweating.
- Children under 6 months of age: 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
Mica, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethiconol/Propylsilsequioxane/Silicate Crosspolymer, Methicone, Maltodextrin, Silica, Glycerin, Club Moss (Lycopodium Clavatum) Extract, Sodium Hyaluronate, Grape (Vitis Vinifera) Seed Extract, Green Tea (Camellia Sinensis) Leaf Extract, Oak (Quercus Robur) Wood Extract, Cogon Grass (Imperata Cylindrica) Root Extract, Water, Tara (Caesalpinia Spinosa) Fruit Pod Extract, Sunflower (Helianthus Annuus) Sprout Extract, Isoceteth-10, Triethoxycaprylylsilane, Sodium Benzoate, Potassium Sorbate, Iron Oxides (CI77491, CI 77492, CI 77499).
- Other information
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 4.3 g Tube Carton
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INGREDIENTS AND APPEARANCE
SUNFORGETTABLE TOTAL PROTECTION SHEET MATTE SUNSCREEN SPF 30
zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68078-036 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 225 mg in 1 g Inactive Ingredients Ingredient Name Strength Mica (UNII: V8A1AW0880) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB) METHICONE (20 CST) (UNII: 6777U11MKT) Maltodextrin (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Glycerin (UNII: PDC6A3C0OX) Isoceteth-10 (UNII: 1K92T9919H) HYALURONATE SODIUM (UNII: YSE9PPT4TH) VITIS VINIFERA SEED (UNII: C34U15ICXA) GREEN TEA LEAF (UNII: W2ZU1RY8B0) QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947) IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH) Water (UNII: 059QF0KO0R) TARA SPINOSA RESIN (UNII: WL3883U2PO) SUNFLOWER OIL (UNII: 3W1JG795YI) Sodium Benzoate (UNII: OJ245FE5EU) Potassium Sorbate (UNII: 1VPU26JZZ4) Triethoxycaprylylsilane (UNII: LDC331P08E) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68078-036-01 1 in 1 CARTON 07/20/2020 1 4.3 g in 1 TUBE, WITH APPLICATOR; 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 07/20/2020 Labeler - Colorescience (128731929)
