Label: STRIVECTIN ANTI-WRINKLE GLOWFECTOR SPF 30- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 76147-240-01, 76147-240-11, 76147-240-91
- Packager: StriVectin Operating Company, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS
- Apply generously 15 minutes before sun exposure and as needed
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time inthe sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPFvalue of 15 or higher and other sun protectionmeasures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats,and sunglasses
- Children under 6 months of age: ask a doctor
- OTHER INFORMATION
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INACTIVE INGREDIENTS
Aqua (Water, Eau), Glycerin, Butyloctyl Salicylate, Dimethicone, Mica, Titanium Dioxide, Diisobutyl Adipate, Polymethylsilsesquioxane/ Silica Crosspolymer, Acrylates/ Dimethicone Copolymer, Fragrance (Parfum), Myristyl Nicotinate, Argania Spinosa (Argan) Kernel Oil, Cocos Nucifera (Coconut) Oil, Ethylhexyl Olivate, Glycine Soja (Soybean) Oil, Brassica Campestris (Rapeseed) Seed Oil, Polysilicone-11, Caprylyl Glycol, Tocopherol, Bis(Cyano Butylacetate) Anthracenediylidene, Sodium Acrylates Copolymer, Phenoxyethanol, Polyglyceryl-3 Diisostearate, Quercus Suber Bark Extract, Polyglyceryl-4 Olivate, Glycyrrhiza Glabra (Licorice) Root Extract, Hexylene Glycol, Oryza Sativa (Rice) Extract, Oryza Sativa (Rice) Germ Extract, Disodium EDTA, Oak Root Extract, Althaea Officinalis Root Extract, Oryza Sativa (Rice) Bran Extract, Retinyl Palmitate, 7-Dehydrocholesterol, Ascorbyl Palmitate, Limonene, Citral, Linalool, Tin Oxide
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STRIVECTIN ANTI-WRINKLE GLOWFECTOR SPF 30
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76147-240 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 7 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) ETHYLHEXYL OLEATE (UNII: R34927QY59) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) COCONUT OIL (UNII: Q9L0O73W7L) MYRISTYL NICOTINATE (UNII: 8QWM6I035C) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIMETHICONE (UNII: 92RU3N3Y1O) SOYBEAN OIL (UNII: 241ATL177A) MICA (UNII: V8A1AW0880) ARGAN OIL (UNII: 4V59G5UW9X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIISOBUTYL ADIPATE (UNII: 8OPY05ZY7S) ORYZA SATIVA WHOLE (UNII: 84IVV0906Z) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CANOLA OIL (UNII: 331KBJ17RK) QUERCUS SUBER BARK (UNII: 8R5219271Q) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) LICORICE (UNII: 61ZBX54883) 2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M) ASCORBYL PALMITATE (UNII: QN83US2B0N) QUERCUS SPP. WHOLE (UNII: MF4E5I2OUQ) ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) LIMONENE, (+)- (UNII: GFD7C86Q1W) CITRAL (UNII: T7EU0O9VPP) LINALOOL, (+)- (UNII: F4VNO44C09) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX) STANNOUS OXIDE (UNII: JB2MV9I3LS) HEXYLENE GLYCOL (UNII: KEH0A3F75J) 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF) TOCOPHEROL (UNII: R0ZB2556P8) ANTHRACENE (UNII: EH46A1TLD7) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76147-240-11 1 in 1 BOX 11/11/2022 1 NDC:76147-240-91 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:76147-240-01 1 mL in 1 PACKET; Type 0: Not a Combination Product 11/11/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/11/2022 Labeler - StriVectin Operating Company, Inc. (832343722) Registrant - StriVectin Operating Company, Inc. (832343722)
