NDC 54868-5680 Taclonex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5680 - Taclonex
Product Packages
NDC Code 54868-5680-0
Package Description: 100 CARTON in 1 CASE / 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 54868-5680?
What are the uses for Taclonex?
Which are Taclonex UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIPOTRIENE HYDRATE (UNII: S7499TYY6G)
- CALCIPOTRIENE (UNII: 143NQ3779B) (Active Moiety)
- BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U)
- BETAMETHASONE (UNII: 9842X06Q6M) (Active Moiety)
Which are Taclonex 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:
- ALPHA-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Taclonex?
- RxCUI: 388525 - calcipotriene 0.005 % / betamethasone dipropionate 0.064 % Topical Ointment
- RxCUI: 388525 - betamethasone 0.0005 MG/MG / calcipotriene 0.00005 MG/MG Topical Ointment
- RxCUI: 388525 - betamethasone 0.05 % (betamethasone dipropionate 0.064 % ) / calcipotriene 0.005 % Topical Ointment
- RxCUI: 388525 - betamethasone 0.05 % / calcipotriene 0.005 % Topical Ointment
- RxCUI: 388525 - betamethasone 0.5 MG (betamethasone dipropionate 0.64 MG) / calcipotriene 0.05 MG per GM Topical Ointment
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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".