NDC 52565-029 Fluocinonide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52565 - Teligent Pharma, Inc.
- 52565-029 - Fluocinonide
Product Packages
NDC Code 52565-029-11
Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE
NDC Code 52565-029-15
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
NDC Code 52565-029-30
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
NDC Code 52565-029-60
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 52565-029?
What are the uses for Fluocinonide?
Which are Fluocinonide UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUOCINONIDE (UNII: 2W4A77YPAN)
- FLUOCINONIDE (UNII: 2W4A77YPAN) (Active Moiety)
Which are Fluocinonide 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2,6-HEXANETRIOL (UNII: W45XXM0XWE)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Fluocinonide?
- RxCUI: 103456 - fluocinonide 0.05 % Topical Cream
- RxCUI: 103456 - fluocinonide 0.5 MG/ML Topical Cream
* 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".