NDC 54868-2861 Alclometasone Dipropionate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2861 - Alclometasone Dipropionate
Product Packages
NDC Code 54868-2861-0
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
NDC Code 54868-2861-1
Package Description: 1 TUBE in 1 CARTON / 45 g in 1 TUBE
Product Details
What is NDC 54868-2861?
What are the uses for Alclometasone Dipropionate?
Which are Alclometasone Dipropionate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCLOMETASONE DIPROPIONATE (UNII: S56PQL4N1V)
- ALCLOMETASONE (UNII: 136H45TB7B) (Active Moiety)
Which are Alclometasone 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- CHLOROCRESOL (UNII: 36W53O7109)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETETH-20 (UNII: I835H2IHHX)
What is the NDC to RxNorm Crosswalk for Alclometasone Dipropionate?
- RxCUI: 855474 - alclometasone dipropionate 0.05 % Topical Cream
- RxCUI: 855474 - alclometasone dipropionate 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".