NDC 54868-5270 Ciclopirox Olamine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5270 - Ciclopirox Olamine
Product Characteristics
Product Packages
NDC Code 54868-5270-0
Package Description: 1 TUBE in 1 CARTON / 90 g in 1 TUBE
NDC Code 54868-5270-1
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
NDC Code 54868-5270-2
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Details
What is NDC 54868-5270?
What are the uses for Ciclopirox Olamine?
Which are Ciclopirox Olamine UNII Codes?
The UNII codes for the active ingredients in this product are:
- CICLOPIROX OLAMINE (UNII: 50MD4SB4AP)
- CICLOPIROX (UNII: 19W019ZDRJ) (Active Moiety)
Which are Ciclopirox Olamine 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- LACTIC ACID (UNII: 33X04XA5AT)
- MINERAL OIL (UNII: T5L8T28FGP)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- WATER (UNII: 059QF0KO0R)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Ciclopirox Olamine?
- RxCUI: 309289 - ciclopirox 0.77 % (ciclopirox olamine 1 % ) Topical Cream
- RxCUI: 309289 - ciclopirox 7.7 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".