NDC 52565-042 Nystatin And Triamcinolone Acetonide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52565 - Teligent Pharma, Inc.
- 52565-042 - Nystatin And Triamcinolone Acetonide
Product Packages
NDC Code 52565-042-15
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
Price per Unit: $0.42771 per GM
NDC Code 52565-042-30
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
Price per Unit: $0.31232 per GM
NDC Code 52565-042-60
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Price per Unit: $0.16620 per GM
Product Details
What is NDC 52565-042?
What are the uses for Nystatin And Triamcinolone Acetonide?
Which are Nystatin And Triamcinolone Acetonide UNII Codes?
The UNII codes for the active ingredients in this product are:
- NYSTATIN (UNII: BDF1O1C72E)
- NYSTATIN (UNII: BDF1O1C72E) (Active Moiety)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (Active Moiety)
Which are Nystatin And 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Nystatin And Triamcinolone Acetonide?
- RxCUI: 1053697 - nystatin 100,000 UNT/GM / triamcinolone acetonide 1 MG/GM Topical Ointment
- RxCUI: 1053697 - nystatin 100 UNT/MG / triamcinolone acetonide 0.001 MG/MG Topical Ointment
- RxCUI: 1053697 - nystatin 100,000 UNT/GM / triamcinolone acetonide 0.1 % Topical Ointment
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Patient Education
Nystatin and Triamcinolone
The combination of nystatin and triamcinolone is used to treat fungal skin infections. It relieves itching, inflammation, and pain. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".