NDC 54868-4907 Halobetasol Propionate
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What is NDC 54868-4907?
What are the uses for Halobetasol Propionate?
Which are Halobetasol Propionate UNII Codes?
The UNII codes for the active ingredients in this product are:
- HALOBETASOL PROPIONATE (UNII: 91A0K1TY3Z)
- HALOBETASOL (UNII: 9P6159HM7T) (Active Moiety)
Which are Halobetasol Propionate 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- STEARETH-21 (UNII: 53J3F32P58)
- WATER (UNII: 059QF0KO0R)
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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".