NDC 76224-101 Spf 15 Self Tanner
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76224-101?
What are the uses for Spf 15 Self Tanner?
Which are Spf 15 Self Tanner UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Spf 15 Self Tanner 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIHYDROXYACETONE (UNII: O10DDW6JOO)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- POMEGRANATE (UNII: 56687D1Z4D)
- PANTHENOL (UNII: WV9CM0O67Z)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALLANTOIN (UNII: 344S277G0Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ROSEMARY (UNII: IJ67X351P9)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CITRAL (UNII: T7EU0O9VPP)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+)- (UNII: F4VNO44C09)
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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".