NDC 21695-201 Clobetasol Propionate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-201 - Clobetasol Propionate
Product Packages
NDC Code 21695-201-15
Package Description: 15 g in 1 TUBE
NDC Code 21695-201-60
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 21695-201?
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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CHLOROCRESOL (UNII: 36W53O7109)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)
- WHITE WAX (UNII: 7G1J5DA97F)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
What is the NDC to RxNorm Crosswalk for Clobetasol Propionate?
- RxCUI: 861448 - clobetasol propionate 0.05 % Topical Ointment
- RxCUI: 861448 - clobetasol propionate 0.0005 MG/MG Topical Ointment
- RxCUI: 861495 - clobetasol propionate 0.05 % Topical Cream
- RxCUI: 861495 - 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".