NDC 72668-001 Zurflex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72668 - Basler Health Care Group
- 72668-001 - Zurflex
Product Packages
NDC Code 72668-001-01
Package Description: 237 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 72668-001?
What are the uses for Zurflex?
Which are Zurflex UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Zurflex 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:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- WATER (UNII: 059QF0KO0R)
- SPEARMINT OIL (UNII: C3M81465G5)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
What is the NDC to RxNorm Crosswalk for Zurflex?
- RxCUI: 1189156 - menthol 9 % Topical Spray
- RxCUI: 1189156 - menthol 90 MG/ML Topical Spray
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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".