NDC 50383-978 Clobetasol Propionate
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50383-978?
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:
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-6 ISOSTEARATE (UNII: 0E2639OTJY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Clobetasol Propionate?
- RxCUI: 861505 - clobetasol propionate 0.05 % Topical Lotion
- RxCUI: 861505 - clobetasol propionate 0.5 MG/ML Topical Lotion
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Patient Education
Clobetasol Topical
Clobetasol topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various scalp and skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body) and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Clobetasol is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
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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".