NDC 50066-701 Cicatricure
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Product Details
What is NDC 50066-701?
What are the uses for Cicatricure?
Which are Cicatricure UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Cicatricure 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- MANNITOL (UNII: 3OWL53L36A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PALMITOYL LYSYLDIOXYMETHIONYLLYSINE (UNII: T7A529FB8O)
- CHAMOMILE (UNII: FGL3685T2X)
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- RICE BRAN OIL (UNII: LZO6K1506A)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- XANTHAN GUM (UNII: TTV12P4NEE)
- NIACINAMIDE (UNII: 25X51I8RD4)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- IMIDUREA (UNII: M629807ATL)
- PANTHENOL (UNII: WV9CM0O67Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".