NDC 81653-008 Regenivade Hair Growth Foam

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
81653-008
Proprietary Name:
Regenivade Hair Growth Foam
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Code:
81653
Start Marketing Date: [9]
11-12-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 81653-008?

The NDC code 81653-008 is assigned by the FDA to the product Regenivade Hair Growth Foam which is product labeled by Guangzhou Jianyuan Biological Technology.co.,ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 81653-008-01 60 ml in 1 bottle , 81653-008-02 180 ml in 1 bottle , 81653-008-03 360 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Regenivade Hair Growth Foam?

●Men: Apply half a capful 2 times a day to the hair loss area. ●Women: Apply half a capful 1 time a day to the hair loss area. ●Massage to area with fingers, then wash hands well. ●Using more and more often will not improve results.

Which are Regenivade Hair Growth Foam UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Regenivade Hair Growth Foam 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:

What is the NDC to RxNorm Crosswalk for Regenivade Hair Growth Foam?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".