Label: STRIVECTIN MULTI-ACTION SUPER-C SPF 30- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 76147-235-11, 76147-235-12
- Packager: StriVectin Operating Company, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 2, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
-
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, Propanediol, Dimethicone, Cetearyl Alcohol, Potassium Cetyl Phosphate, Tetrahexyldecyl Ascorbate, Ergothioneine, Mannitol, Bacillus/Sea Salt, Ferment Filtrate, Myristyl Nicotinate, Citrus Japonica Fruit Extract, Oryza Sativa (Rice) Germ Extract, Morinda Citrifolia Extract, Oryza Sativa (Rice) Extract, Glycerin,Glycerin Soja (Soybean) Oil, Tocopheryl Acetate, Cetearyl Glucoside, Lecithin, Ubiquinone, Butylene Glycol, 1,2 Hexanediol, Decyl Glucoside, Hexylene Gkycik, CaprylylGlycol, Polysilicon-11, Polyglyceritl-3 Diisostearate, Acrylates/C 10-30Alkyl Acrylate Crosspolymer, Sodium Acrylates Copolymer, Caprylhydroamic Acid, Aminomethyl Propanol, Disodium EDTA, Fragrance/Parfum, Phenoxyethanol, Sodium Benzoate, Citric Acid, Limonene, Linalool, Benzyl Benzoate, Geraniol, Citral, Yellow 5 (CI 19140), Red 40 (CI 16035), [ILN 60988]
- 01b UC Super-C SPF 30 50mL.
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INGREDIENTS AND APPEARANCE
STRIVECTIN MULTI-ACTION SUPER-C SPF 30
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76147-235 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 WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE (UNII: 92RU3N3Y1O) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) ERGOTHIONEINE (UNII: BDZ3DQM98W) MANNITOL (UNII: 3OWL53L36A) SEA SALT (UNII: 87GE52P74G) MYRISTYL NICOTINATE (UNII: 8QWM6I035C) CITRUS JAPONICA FRUIT (UNII: 8PS197OFKT) RICE GERM (UNII: 7N2B70SFEZ) NONI FRUIT (UNII: 7829X3G2X5) RICE OIL (UNII: ACU8G2V809) GLYCERIN (UNII: PDC6A3C0OX) SOYBEAN OIL (UNII: 241ATL177A) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) UBIQUINOL (UNII: M9NL0C577Y) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYSILICONE-15 (UNII: F8DRP5BB29) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3) SODIUM ACRYLATE (UNII: 7C98FKB43H) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) CITRIC ACID ACETATE (UNII: DSO12WL7AU) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+)- (UNII: F4VNO44C09) BENZYL BENZOATE (UNII: N863NB338G) GERANIOL (UNII: L837108USY) CITRAL (UNII: T7EU0O9VPP) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76147-235-11 1 in 1 BOX 04/22/2021 1 50 mL in 1 JAR; Type 0: Not a Combination Product 2 NDC:76147-235-12 1 in 1 BOX 04/22/2021 2 30 mL in 1 JAR; 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 04/22/2021 Labeler - StriVectin Operating Company, Inc. (832343722) Registrant - StriVectin Operating Company, Inc. (832343722)
