Label: RIMMEL LONDON MATCH PERFECTION FOUNDATION - NATURAL BEIGE (440)- octinoxate, titanium dioxide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 59351-0328-1 - Packager: Lancaster S.A.M.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 October 6, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DESCRIPTION
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
COSMETIC INGREDIENTS: AQUA/
WATER/EAU, CYCLOPENTASILOXANE,
TALC, GLYCERIN, CETYL PEG/
PPG-10/1 DIMETHICONE, ISONONYL
ISONONANOATE, PHENYL
TRIMETHICONE, HYDROGENATED
POLYISOBUTENE, SILICA DIMETHYL
SILYLATE, PROPYLENE GLYCOL,
TRIETHYLHEXANOIN, CALCIUM
ALUMINUM BOROSILICATE,
MAGNESIUM SULFATE, SODIUM
GLUTAMATE, TRIBEHENIN, BIS-PEG/
PPG-14/14 DIMETHICONE,
DIMETHICONE, LECITHIN,
DISTEARDIMONIUM HECTORITE,
DIPHENYL DIMETHICONE, LAURETH-7,
PARFUM/FRAGRANCE, MICA,
PHENOXYETHANOL, METHYLPARABEN,
PROPYLPARABEN, METHYL
METHACRYLATE CROSSPOLYMER,
DISODIUM STEAROYL GLUTAMATE,
PROPYLENE CARBONATE, C12-15
ALKYL BENZOATE, DISODIUM
EDTA, ALUMINUM HYDROXIDE,
SILICA, ASCORBYL GLUCOSIDE,
SODIUM HYALURONATE,
THYMUS SERPILLUM EXTRACT,
CERAMIDE 2, PEG-10 RAPESEED
STEROL, BIOSACCHARIDE GUM-1,
BHT, LUPINUS ALBUS SEED
EXTRACT, SAPPHIRE POWDER,
BUTYLPARABEN, ETHYLPARABEN,
PALMITOYL OLIGOPEPTIDE,
TOCOPHEROL, ISOBUTYLPARABEN,
[May Contain/Peut Contenir:
TITANIUM DIOXIDE (CI 77891),
IRON OXIDES (CI 77491,
CI 77492, CI77499)]. - INDICATIONS & USAGE
- WARNINGS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RIMMEL LONDON MATCH PERFECTION FOUNDATION - NATURAL BEIGE (440)
octinoxate, titanium dioxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59351-0328 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 1.2 mL in 30 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.9 mL in 30 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) TALC (UNII: 7SEV7J4R1U) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U) TRIBEHENIN (UNII: 8OC9U7TQZ0) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) HECTORITE (UNII: 08X4KI73EZ) LAURETH-7 (UNII: Z95S6G8201) MICA (UNII: V8A1AW0880) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYL METHACRYLATE (UNII: 196OC77688) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) EDETATE DISODIUM (UNII: 7FLD91C86K) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) THYMUS (UNII: 9CC998Z1E1) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) BUTYLPARABEN (UNII: 3QPI1U3FV8) ETHYLPARABEN (UNII: 14255EXE39) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) IRON (UNII: E1UOL152H7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59351-0328-1 30 mL in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 10/06/2010 Labeler - Lancaster S.A.M. (401011325) Registrant - Rimmel Inc. (965020402) Establishment Name Address ID/FEI Business Operations Lancaster S.A.M. 401011325 manufacture