NDC 42254-322 Nystatin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42254 - Rebel Distributors Corp
- 42254-322 - Nystatin
Product Characteristics
PEPPERMINT (C73408)
Product Packages
NDC Code 42254-322-60
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 42254-322?
What are the uses for Nystatin?
Which are Nystatin UNII Codes?
The UNII codes for the active ingredients in this product are:
- NYSTATIN (UNII: BDF1O1C72E)
- NYSTATIN (UNII: BDF1O1C72E) (Active Moiety)
Which are Nystatin 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:
- SUCROSE (UNII: C151H8M554)
- ALCOHOL (UNII: 3K9958V90M)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Nystatin?
- RxCUI: 312055 - nystatin 100,000 UNT/mL Oral Suspension
- RxCUI: 312055 - nystatin 100000 UNT/ML Oral Suspension
- RxCUI: 312055 - nystatin 100,000 UNT/ML Oral Suspension
- RxCUI: 312055 - nystatin 500,000 UNT per 5 ML Oral Suspension
* 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".