Label: BEAUTY DYNAMICS SPF 15 DAILY EYE TREATMENT- avobenzone, homosalate, octisalate, octocrylene cream
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Contains inactivated NDC Code(s)
NDC Code(s): 68828-072-01, 68828-072-02 - Packager: JAFRA COSMETICS INTERNATIONAL
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 18, 2012
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ACTIVE INGREDIENT
Sunscreen Active Ingredients (SPF 15): Butyl methoxydibenzoylmethane/Avobenzene, Homosalate, Octisalate/Ethylhexyl Salicylate, Octocrylene
Water/Aqua, Niacinamide, Fraxinus Exelsior Bark Extract, Silanetriol, Potassium Citrate, Butylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyltaurate Copolymer, Squalane, Polysorbate 60, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Laminaria Ochroleuca Extract, Panthenol, Glycerin, Palmitoyl Dipeptide-5, Diaminobutyloyl Hydroxythreonine, Palmitoyl Dipeptide-6 Diaminohydroxybutyrate, Bisabolol, DMDM Hydantoin, Allantoin, Tocopheryl Acetate, PEG-4 Laurate, Iodopropynyl Butylcarbamate, Trisodium EDTA.
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INGREDIENTS AND APPEARANCE
BEAUTY DYNAMICS SPF 15 DAILY EYE TREATMENT
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68828-072 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.5 mL in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 7.5 mL in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 mL in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 1.75 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) FRAXINUS EXCELSIOR BARK (UNII: R6KCX5H8I2) SILANETRIOL (UNII: E52D0J3TS5) POTASSIUM CITRATE (UNII: EE90ONI6FF) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) POLYSORBATE 60 (UNII: CAL22UVI4M) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) LAMINARIA OCHROLEUCA (UNII: 4R2124HE76) PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) LEVOMENOL (UNII: 24WE03BX2T) DMDM HYDANTOIN (UNII: BYR0546TOW) ALLANTOIN (UNII: 344S277G0Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PEG-4 LAURATE (UNII: AYF4VM3N1Z) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) EDETATE TRISODIUM (UNII: 420IP921MB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68828-072-02 1 in 1 BOX 1 NDC:68828-072-01 15 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/18/2012 Labeler - JAFRA COSMETICS INTERNATIONAL (041676479) Registrant - JAFRA COSMETICS INTERNATIONAL (041676479) Establishment Name Address ID/FEI Business Operations Jafra Manufacturing, S.A. de C.V. 814732061 manufacture
