NDC 50653-3001 Bonogen Activator Hair Loss Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50653 - Bonogen Co., Ltd
- 50653-3001 - Bonogen Activator
Product Packages
NDC Code 50653-3001-1
Package Description: 100 mL in 1 BOTTLE, WITH APPLICATOR
NDC Code 50653-3001-2
Package Description: 150 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 50653-3001?
Which are Bonogen Activator Hair Loss Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Bonogen Activator Hair Loss Treatment?
- RxCUI: 1044988 - biotin 0.002 % Topical Solution
- RxCUI: 1044988 - biotin 0.02 MG/ML Topical Solution
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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".