NDC 70493-984 Wonder Glow Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70493-984?
Which are Wonder Glow Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Wonder Glow Cream 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- GUM TALHA (UNII: H18F76G097)
- HYALURONIC ACID (UNII: S270N0TRQY)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- WATER (UNII: 059QF0KO0R)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GERANIOL (UNII: L837108USY)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM ISOSTEARATE (UNII: 8WF2JE0F41)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- OCTISALATE (UNII: 4X49Y0596W)
- HOMOSALATE (UNII: V06SV4M95S)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- EUGENOL (UNII: 3T8H1794QW)
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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".