Label: FLAWLESS BY SONYA ALOE BB CREME COCOA- titanium dioxide cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 11697-373-01, 11697-373-02 - Packager: Aloe Vera of America, Inc.
- 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 January 13, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses
- WARNINGS
- Directions
-
INACTIVE INGREDIENT
Inactive Ingredients
water/aqua/eau, dimethicone, coco-caprylate, dimethicone/vinyl dimethicone crosspolymer, talc, iron oxides (CI 77491, CI 77492, CI 77499), caprylic/capric triglyceride, cetyl peg/ppg-10/1 dimethicone, propanediol, butylene glycol, sorbitan olivate, glyceryl tribehante/isostearate/eicosandioate, titanium dioxide (CI 77891), stearalkonium hectorite, mica, sodium chloride, phenoxyethanol, tropolone, sodium dehydroacetate, propylene carbonate, hydrogen dimethicone, alumina, enantia chlorantha bark extract, triethoxycaprylylsilane, aloe barbadensis leaf extract, fragrance/parfum, tin oxide, olea europaea (olive) leaf extract, trisodium ethylenediamine disuccinate, alcohol, maltodextrin, olea europaea (olive) fruit extract, oleanolic acid.
- Other Information
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FLAWLESS BY SONYA ALOE BB CREME COCOA
titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11697-373 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1.3500 g in 45.0000 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) COCO-CAPRYLATE (UNII: 4828G836N6) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) TALC (UNII: 7SEV7J4R1U) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP) PROPANEDIOL (UNII: 5965N8W85T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SORBITAN OLIVATE (UNII: MDL271E3GR) GLYCERYL TRIBEHENATE/ISOSTEARATE/EICOSANDIOATE (UNII: 3Y9NJ5Z7E5) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) MICA (UNII: V8A1AW0880) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) TROPOLONE (UNII: 7L6DL16P1T) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) PROPYLENE CARBONATE (UNII: 8D08K3S51E) METHICONE (20 CST) (UNII: 6777U11MKT) ALUMINUM OXIDE (UNII: LMI26O6933) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ALOE VERA LEAF (UNII: ZY81Z83H0X) STANNIC OXIDE (UNII: KM7N50LOS6) OLEA EUROPAEA BARK (UNII: 4BN4L34UKC) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) ALCOHOL (UNII: 3K9958V90M) MALTODEXTRIN (UNII: 7CVR7L4A2D) BLACK OLIVE (UNII: 2M6QWV94OC) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11697-373-02 1 in 1 CARTON 1 NDC:11697-373-01 45 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/01/2013 Labeler - Aloe Vera of America, Inc. (049049463) Registrant - Aloe Vera of America, Inc. (049049463) Establishment Name Address ID/FEI Business Operations Aloe Vera of America, Inc. 049049463 manufacture(11697-373)