NDC 55891-001 Flawless By Sonya Aloe Bb Creme Nude Spf 20 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55891 - Forever Living Products
- 55891-001 - Flawless By Sonya Aloe Bb Creme Nude Spf 20 Sunscreen
Product Packages
NDC Code 55891-001-00
Package Description: 1 TUBE in 1 BOX / 45 g in 1 TUBE
Product Details
What is NDC 55891-001?
What are the uses for Flawless By Sonya Aloe Bb Creme Nude Spf 20 Sunscreen?
Which are Flawless By Sonya Aloe Bb Creme Nude Spf 20 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 Nude Spf 20 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- TALC (UNII: 7SEV7J4R1U)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- PROPANEDIOL (UNII: 5965N8W85T)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROPOLONE (UNII: 7L6DL16P1T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ACMELLA OLERACEA FLOWER (UNII: 2794N5KM0K)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- ALCOHOL (UNII: 3K9958V90M)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- BLACK OLIVE (UNII: 2M6QWV94OC)
* Please review the disclaimer below.
[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".