NDC 68078-016 Bronzing Perfector Spf 20 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68078-016?
What are the uses for Bronzing Perfector Spf 20 Sunscreen?
Which are Bronzing Perfector 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Bronzing Perfector 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL HYDROXYSTEARATE BENZOATE (UNII: 3W8F25684B)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- MICA (UNII: V8A1AW0880)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- RICE BRAN (UNII: R60QEP13IC)
- OAT (UNII: Z6J799EAJK)
- SPIRULINA MAXIMA (UNII: 9K7IG15M0Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DULSE (UNII: 7832HOY4ZQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYSACCHARIDE-K (UNII: 3X48A86C8K)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- JOJOBA OIL (UNII: 724GKU717M)
- TEA TREE OIL (UNII: VIF565UC2G)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MANDARIN OIL (UNII: NJO720F72R)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CALCIUM SILICATE (UNII: S4255P4G5M)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
* 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".