NDC 50090-2055 Triamcinolone Acetonide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-2055 - Triamcinolone Acetonide
Product Packages
NDC Code 50090-2055-0
Package Description: 15 g in 1 TUBE
Product Details
What is NDC 50090-2055?
What are the uses for Triamcinolone Acetonide?
Which are Triamcinolone Acetonide UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (Active Moiety)
Which are Triamcinolone Acetonide 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 40 (UNII: STI11B5A2X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- WATER (UNII: 059QF0KO0R)
- SORBIC ACID (UNII: X045WJ989B)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MINERAL OIL (UNII: T5L8T28FGP)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
What is the NDC to RxNorm Crosswalk for Triamcinolone Acetonide?
- RxCUI: 1085644 - triamcinolone acetonide 0.025 % Topical Cream
- RxCUI: 1085644 - triamcinolone acetonide 0.25 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".