NDC 44781-190 Rebirth Hair Tonic

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:
44781-190
Proprietary Name:
Rebirth Hair Tonic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zion Synthetic Fiber Co., Ltd.
Labeler Code:
44781
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44781-190-01

Package Description: 130 mL in 1 CARTON

Product Details

What is NDC 44781-190?

The NDC code 44781-190 is assigned by the FDA to the product Rebirth Hair Tonic which is product labeled by Zion Synthetic Fiber Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44781-190-01 130 ml in 1 carton . 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 Rebirth Hair Tonic?

Indication and usage:Tighten the lid after using it.Don't keep it in the place where the temperature is extremely hot or low and exposed the direct sunlight.    Use it after Rebirth Hair Shampoo.

Which are Rebirth Hair Tonic UNII Codes?

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

Which are Rebirth Hair Tonic 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".