NDC 42248-105 Retin C
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 42248-105?
Which are Retin C UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Retin C 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:
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ALOE (UNII: V5VD430YW9)
- WATER (UNII: 059QF0KO0R)
- EPILOBIUM ANGUSTIFOLIUM LEAF (UNII: 7NV86426N2)
- LEMON JUICE (UNII: AGN709ANTJ)
- BUTYL ESTER OF METHYL VINYL ETHER-MALEIC ANHYDRIDE COPOLYMER (125 KD) (UNII: 389H2R62BD)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TALC (UNII: 7SEV7J4R1U)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- SODIUM ASCORBATE (UNII: S033EH8359)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- TRICLOSAN (UNII: 4NM5039Y5X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".