Label: VICHY LABORATOIRES CAPITAL SOLEIL 50 DAILY ANTIAGING FACE SUNSCREEN BROAD SPECTRUM SPF 50 WATER RESISTANT 80 MINUTES- avobenzone, homosalate, octisalate and octocrylene lotion
- NDC Code(s): 49967-054-01, 49967-054-02
- Packager: L’Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
● apply liberally 15 minutes before sun exposure
● reapply:
● after 80 minutes of swimming or sweating
● immediately after towel drying
● at least every 2 hours
● 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
● children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
water, cyclopentasiloxane, alcohol denat., silica, dicaprylyl ether, styrene/acrylates copolymer, PEG-30 dipolyhydroxystearate, dimethicone, cyclohexasiloxane, polymethylsilsesquioxane, glycerin, nylon-12, butylene glycol, caprylyl glycol, citric acid, dicaprylyl carbonate, disodium EDTA, disteardimonium hectorite, fragrance, isostearyl alcohol, lauryl PEG/PPG-18/18 methicone, p-anisic acid, PEG-8 laurate, phenoxyethanol, poly c10-30 alkyl acrylate, potassium sorbate, propylene carbonate, sodium benzoate, sodium chloride, sodium dodecylbenzenesulfonate, tocopherol,
vitis vinifera (grape) fruit extract - Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VICHY LABORATOIRES CAPITAL SOLEIL 50 DAILY ANTIAGING FACE SUNSCREEN BROAD SPECTRUM SPF 50 WATER RESISTANT 80 MINUTES
avobenzone, homosalate, octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-054 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DICAPRYLYL ETHER (UNII: 77JZM5516Z) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 6 (UNII: XHK3U310BA) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) GLYCERIN (UNII: PDC6A3C0OX) NYLON-12 (UNII: 446U8J075B) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) P-ANISIC ACID (UNII: 4SB6Y7DMM3) PEG-8 LAURATE (UNII: 762O8IWA10) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPYLENE CARBONATE (UNII: 8D08K3S51E) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) TOCOPHEROL (UNII: R0ZB2556P8) WINE GRAPE (UNII: 3GOV20705G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-054-01 1 in 1 CARTON 05/01/2020 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-054-02 1 in 1 CARTON 05/01/2020 05/01/2020 2 50 mL in 1 TUBE; 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 05/01/2020 Labeler - L’Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L’Oreal USA, Inc. 185931458 analysis(49967-054) Establishment Name Address ID/FEI Business Operations Goodier Cosmetics 007317209 manufacture(49967-054)
