NDC 0168-0314 Ciclopirox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0168 - E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.
- 0168-0314 - Ciclopirox
Product Packages
Product Details
What is NDC 0168-0314?
What are the uses for Ciclopirox?
Which are Ciclopirox 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 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:
- WATER (UNII: 059QF0KO0R)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- MINERAL OIL (UNII: T5L8T28FGP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- LACTIC ACID (UNII: 33X04XA5AT)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
What is the NDC to RxNorm Crosswalk for Ciclopirox?
- RxCUI: 309290 - ciclopirox 0.77 % Topical Lotion
- RxCUI: 309290 - ciclopirox 7.7 MG/ML Topical Lotion
- RxCUI: 309290 - ciclopirox 0.77 % (ciclopirox olamine 1 % ) Topical Lotion
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Patient Education
Ciclopirox Topical
Ciclopirox topical solution is used along with regular nail trimming to treat fungal infections of the fingernails and toenails (an infection that may cause nail discoloration, splitting and pain). Ciclopirox is in a class of medications called antifungals. It works by stopping the growth of nail fungus.
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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".