NDC 61360-1351 Ciclopirox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61360 - Taro Pharmaceuticals, Inc.
- 61360-1351 - Ciclopirox
Product Packages
NDC Code 61360-1351-8
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 120 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61360-1351?
What are the uses for Ciclopirox?
Which are Ciclopirox UNII Codes?
The UNII codes for the active ingredients in this product are:
- CICLOPIROX (UNII: 19W019ZDRJ)
- 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:
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- LAURETH-2 (UNII: D4D38LT1L5)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
What is the NDC to RxNorm Crosswalk for Ciclopirox?
- RxCUI: 250344 - ciclopirox 1 % Medicated Shampoo
- RxCUI: 250344 - ciclopirox 10 MG/ML Medicated Shampoo
* 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".