NDC 72934-4075 Finasteride 0.1% / Minoxidil 7%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72934 - Sincerus Florida, Llc
- 72934-4075 - Finasteride 0.1% / Minoxidil 7%
Product Characteristics
Product Packages
NDC Code 72934-4075-8
Package Description: 60 g in 1 BOTTLE, GLASS
Product Details
What is NDC 72934-4075?
Which are Finasteride 0.1% / Minoxidil 7% UNII Codes?
The UNII codes for the active ingredients in this product are:
- FINASTERIDE (UNII: 57GNO57U7G)
- FINASTERIDE (UNII: 57GNO57U7G) (Active Moiety)
- MINOXIDIL (UNII: 5965120SH1)
- MINOXIDIL (UNII: 5965120SH1) (Active Moiety)
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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".