NDC 83104-401 Arca Regnerationshampoo

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:
83104-401
Proprietary Name:
Arca Regnerationshampoo
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hair Arca, Inc
Labeler Code:
83104
Start Marketing Date: [9]
10-04-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 83104-401-01

Package Description: 503 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 83104-401?

The NDC code 83104-401 is assigned by the FDA to the product Arca Regnerationshampoo which is product labeled by Hair Arca, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83104-401-01 503 ml in 1 bottle, pump . 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 Arca Regnerationshampoo?

ARCA REGENRATION SHAMPOO recommends the following instructions for scalp improvement and skin troubles. 1 Wet your hair and scalp completely with clean warm water before shampoo 2 Use 1-3 shampoo pumps to massage your scalp and hair. Then wait 2 to 3 minutes. 3 Rinse thoroughly with warm water. (Head spa is recommended after hair shampoo use)

Which are Arca Regnerationshampoo UNII Codes?

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

Which are Arca Regnerationshampoo 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:

* Please review the disclaimer below.

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".