Label: PEACH SAKE PORE BB SPF20 PA PLUS NUMBER1 LIGHT BEIGE- titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 76214-017-01 - Packager: SKINFOOD CO., LTD.
- 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 September 7, 2011
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, PEG/PPG-19/19 DIMETHICONE, BARIUM SULFATE, CAPRYLYL METHICONE, CETYL PEG/PPG-10/1 DIMETHICONE, SODIUM CHLORIDE, CYCLOHEXASILOXANE, POLYMETHYL METHACRYLATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, DIMETHICONE, SORBITAN ISOSTEARATE, POLYQUATERNIUM-51, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, STEARIC ACID, SORBITAN OLIVATE, TRIMETHYLSILOXYSILICATE, PROPYLENE CARBONATE, TRIETHOXYCAPRYLYLSILANE, PRUNUS PERSICA (PEACH) FRUIT EXTRACT, RICE FERMENT FILTRATE (SAKE), ENANTIA CHLORANTHA BARK EXTRACT, OLEANOLIC ACID, ALCOHOL, TALC, PHENOXYETHANOL, PROPYLPARABEN, METHYLPARABEN, FRAGRANCE, IRON OXIDES (CI 77492), IRON OXIDES (CI 77491), IRON OXIDES (CI 77499), ULTRAMARINES (CI 77007) - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PEACH SAKE PORE BB SPF20 PA PLUS NUMBER1 LIGHT BEIGE
titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76214-017 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 2.32 mL in 30 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.9 mL in 30 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BARIUM SULFATE (UNII: 25BB7EKE2E) SODIUM CHLORIDE (UNII: 451W47IQ8X) CYCLOMETHICONE 6 (UNII: XHK3U310BA) DIMETHICONE (UNII: 92RU3N3Y1O) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) SORBITAN OLIVATE (UNII: MDL271E3GR) PROPYLENE CARBONATE (UNII: 8D08K3S51E) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEACH (UNII: 3OKE88I3QG) TALC (UNII: 7SEV7J4R1U) ALCOHOL (UNII: 3K9958V90M) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76214-017-01 30 mL in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 03/01/2011 Labeler - SKINFOOD CO., LTD. (690324173) Registrant - SKINFOOD CO., LTD. (690324173) Establishment Name Address ID/FEI Business Operations SKINFOOD CO., LTD. 690324173 manufacture