NDC 54868-5692 Betamethasone Dipropionate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5692 - Betamethasone Dipropionate
Product Packages
NDC Code 54868-5692-0
Package Description: 15 g in 1 TUBE
Product Details
What is NDC 54868-5692?
What are the uses for Betamethasone Dipropionate?
Which are Betamethasone Dipropionate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U)
- BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (Active Moiety)
Which are Betamethasone Dipropionate 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)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Betamethasone Dipropionate?
- RxCUI: 848208 - betamethasone dipropionate 0.05 % Augmented Topical Gel
- RxCUI: 848208 - Augmented betamethasone 0.0005 MG/MG Topical Gel
- RxCUI: 848208 - augmented betamethasone 0.05 % Topical Gel
- RxCUI: 848208 - betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) Augmented Topical Gel
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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".