NDC 54473-174 Spf 15 Fair
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54473-174?
Which are Spf 15 Fair 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 Spf 15 Fair 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:
- MICA (UNII: V8A1AW0880)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- KAOLIN (UNII: 24H4NWX5CO)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HYALURONIC ACID (UNII: S270N0TRQY)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- UREA (UNII: 8W8T17847W)
- TREHALOSE (UNII: B8WCK70T7I)
- TRIACETIN (UNII: XHX3C3X673)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- GLYCINE (UNII: TE7660XO1C)
- CHONDROITIN SULFATE (PORCINE) (UNII: V5E8ELO4W9)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ORNITHINE HYDROCHLORIDE (UNII: HBK84K66XH)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* 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".