NDC 57975-161 Regeneration Wrinkle Control Cream Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57975-161?
Which are Regeneration Wrinkle Control Cream Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Regeneration Wrinkle Control Cream Spf 15 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)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- XYLITOL (UNII: VCQ006KQ1E)
- CREATININE (UNII: AYI8EX34EU)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)
- POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
- DOCOSANOL (UNII: 9G1OE216XY)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- PANTHENOL (UNII: WV9CM0O67Z)
- ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- TEA LEAF (UNII: GH42T47V24)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- BIOTIN (UNII: 6SO6U10H04)
- HEXAPEPTIDE-10 (UNII: W9RS1K7T9I)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARBOMER 934 (UNII: Z135WT9208)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
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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".