Label: ALOE SUN BB SPF20 PA PLUS NUMBER1 NATURAL SKIN- titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 76214-028-01 - Packager: SKINFOOD 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 September 23, 2011
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
WATER, CYCLOPENTASILOXANE, CETYL PEG/PPG-10/1 DIMETHICONE, BUTYLENE GLYCOL, POLYMETHYL METHACRYLATE, CERESIN, BORON NITRIDE, SORBITAN ISOSTEARATE, SODIUM CHLORIDE, DIMETHICONE, PHENYL TRIMETHICONE, SORBITAN OLIVATE, SILICA, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ALOE BARBADENSIS LEAF EXTRACT, TRIMETHYLSILOXYSILICATE, ALUMINUM HYDROXIDE, STEARIC ACID, TRIETHOXYCAPRYLYLSILANE, TALC, METHYLPARABEN, PHENOXYETHANOL, PROPYLPARABEN, FRAGRANCE, IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), ULTRAMARINES (CI 77007), IRON OXIDES (CI 77491) - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALOE SUN BB SPF20 PA PLUS NUMBER1 NATURAL SKIN
titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76214-028 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 3.86 g in 50 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 1.5 g in 50 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CERESIN (UNII: Q1LS2UJO3A) BORON NITRIDE (UNII: 2U4T60A6YD) SODIUM CHLORIDE (UNII: 451W47IQ8X) DIMETHICONE (UNII: 92RU3N3Y1O) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) SORBITAN OLIVATE (UNII: MDL271E3GR) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) METHYLPARABEN (UNII: A2I8C7HI9T) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLPARABEN (UNII: Z8IX2SC1OH) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76214-028-01 50 g 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