NDC 23637-002 Advanced Herbal Care For Thinning-damaged Hair

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
23637-002
Proprietary Name:
Advanced Herbal Care For Thinning-damaged Hair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
B'iota Laboratories
Labeler Code:
23637
Start Marketing Date: [9]
01-16-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 23637-002-01

Package Description: 1 BOTTLE in 1 CARTON / 300 mL in 1 BOTTLE

Product Details

What is NDC 23637-002?

The NDC code 23637-002 is assigned by the FDA to the product Advanced Herbal Care For Thinning-damaged Hair which is product labeled by B'iota Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 23637-002-01 1 bottle in 1 carton / 300 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 Advanced Herbal Care For Thinning-damaged Hair?

Helps eliminate and reduces the recurrence of scalp itching, irritation, redness, flaking and scaling associated with dandruff.

Which are Advanced Herbal Care For Thinning-damaged Hair UNII Codes?

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

Which are Advanced Herbal Care For Thinning-damaged Hair 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:

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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".