NDC 65179-501 Desoximetasone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65179 - Groupe Parima Inc
- 65179-501 - Desoximetasone
Product Packages
NDC Code 65179-501-15
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
NDC Code 65179-501-60
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 65179-501?
What are the uses for Desoximetasone?
Which are Desoximetasone UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESOXIMETASONE (UNII: 4E07GXB7AU)
- DESOXIMETASONE (UNII: 4E07GXB7AU) (Active Moiety)
Which are Desoximetasone 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 HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Desoximetasone?
- RxCUI: 315059 - desoximetasone 0.05 % Topical Gel
- RxCUI: 315059 - desoximetasone 0.0005 MG/MG Topical Gel
- RxCUI: 315059 - desoximetasone 0.5 MG per GM Topical Gel
* Please review the disclaimer below.
[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".