NDC 55891-002 Flawless By Sonya Aloe Bb Creme Cocoa Spf 10 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 55891-002?
What are the uses for Flawless By Sonya Aloe Bb Creme Cocoa Spf 10 Sunscreen?
Which are Flawless By Sonya Aloe Bb Creme Cocoa Spf 10 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Flawless By Sonya Aloe Bb Creme Cocoa Spf 10 Sunscreen Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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 5) (UNII: 035JKJ76MT)
- PROPANEDIOL (UNII: 5965N8W85T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- MICA (UNII: V8A1AW0880)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROPOLONE (UNII: 7L6DL16P1T)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- ALCOHOL (UNII: 3K9958V90M)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".