Label: FACE IT HD PERFECT BB SPF30 PA 02- octinoxate, titanium dioxide, zinc oxide, betaine, talc cream
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Contains inactivated NDC Code(s)
NDC Code(s): 51523-104-01, 51523-104-02 - Packager: THEFACESHOP CO., LTD
- Category: HUMAN OTC DRUG LABEL
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 August 23, 2011
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ACTIVE INGREDIENT
OCTINOXATE (6%)
TITANIUM DIOXIDE (6.36%)
ZINC OXIDE (2.88%)
BETAINE (2%)
TALC (0.684%)WATER, CYCLOMETHICONE, DIPROPYLENE GLYCOL, DIMETHICONE, GLYCERIN, MICA, TITANIUM DIOXIDE, ALUMINUM HYDROXIDE, STEARIC ACID, DIMETHICONE, MAGNESIUM SULFATE, TRIETHOXYCAPRYLYLSILANE, POLYGLYCERYL-4 ISOSTEARATE, HEXYL LAURATE, PHENOXYETHANOL, TRIETHOXYCAPRYLYLSILANE, METHYLPARABEN, DISTEARYLDIMONIUM CHLORIDE, STEARIC ACID, CAREX HUMILIS ROOT, ETHYLPARABEN, PROPYLPARABEN, MICA, TRIETHYLHEXANOIN, MARITIME PINE
- PURPOSE
- WHEN USING
- STOP USE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FACE IT HD PERFECT BB SPF30 PA 02
octinoxate, titanium dioxide, zinc oxide, betaine, talc creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51523-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6 mL in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 6.36 mL in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 2.88 mL in 100 mL BETAINE (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W) BETAINE 2 mL in 100 mL TALC (UNII: 7SEV7J4R1U) (TALC - UNII:7SEV7J4R1U) TALC 0.684 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) DIPROPYLENE GLYCOL (UNII: E107L85C40) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) DIMETHICONE (UNII: 92RU3N3Y1O) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) HEXYL LAURATE (UNII: 4CG9F9W01Q) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) METHYLPARABEN (UNII: A2I8C7HI9T) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) STEARIC ACID (UNII: 4ELV7Z65AP) CAREX HUMILIS ROOT (UNII: QFR9QY5U3V) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) MICA (UNII: V8A1AW0880) TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K) MARITIME PINE (UNII: 50JZ5Z98QY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51523-104-02 1 in 1 BOX 1 NDC:51523-104-01 40 mL in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/23/2011 Labeler - THEFACESHOP CO., LTD (688329416) Registrant - THEFACESHOP CO., LTD (688329416) Establishment Name Address ID/FEI Business Operations THEFACESHOP CO., LTD 688329416 manufacture