NDC 54868-6305 Clobetasol Propionate
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What is NDC 54868-6305?
What are the uses for Clobetasol Propionate?
Which are Clobetasol Propionate UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOBETASOL PROPIONATE (UNII: 779619577M)
- CLOBETASOL (UNII: ADN79D536H) (Active Moiety)
Which are Clobetasol 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:
- CETETH-20 (UNII: I835H2IHHX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- IMIDUREA (UNII: M629807ATL)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
What is the NDC to RxNorm Crosswalk for Clobetasol Propionate?
- RxCUI: 1992281 - clobetasol propionate 0.05 % Emollient Base Topical Cream
- RxCUI: 1992281 - Emollient clobetasol propionate 0.5 MG/ML Topical Cream
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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".