NDC 72904-001 Iasobetic Allantoin Skin Protectant
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What is NDC 72904-001?
What are the uses for Iasobetic Allantoin Skin Protectant?
Which are Iasobetic Allantoin Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Iasobetic Allantoin Skin Protectant 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SHEA BUTTER (UNII: K49155WL9Y)
- TURMERIC (UNII: 856YO1Z64F)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- GLYCOL STEARATE SE (UNII: 6YLY96TQL6)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LAURETH-8 (UNII: QU7U88D04I)
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".