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NDC 70878-001 Regrowz Homeopathic Scalp Stimulant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70878-001?
  4. Regrowz Homeopathic Scalp Stimulant Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70878-001
Proprietary Name:
Regrowz Homeopathic Scalp Stimulant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Regrowz Ltd
Labeler Code:
70878
Product Label ID:
38b7f9b5-7fc8-11eb-e054-00144ff8d46c
Start Marketing Date: [9]
07-28-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70878-001-01

Package Description: 25 mg in 1 SYRINGE, GLASS

Product Details

What is NDC 70878-001?

The NDC code 70878-001 is assigned by the FDA to the product Regrowz Homeopathic Scalp Stimulant which is product labeled by Regrowz Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70878-001-01 25 mg in 1 syringe, glass . 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 Regrowz Homeopathic Scalp Stimulant?

Uses Promotes hair re-growth Prevents or reduces hair loss Thickens existing hair

Which are Regrowz Homeopathic Scalp Stimulant UNII Codes?

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

Which are Regrowz Homeopathic Scalp Stimulant 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".