NDC 70937-100 Eh Hair Plus Regeneration Hair Care

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:
70937-100
Proprietary Name:
Eh Hair Plus Regeneration Hair Care
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70937
Start Marketing Date: [9]
08-25-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70937-100?

The NDC code 70937-100 is assigned by the FDA to the product Eh Hair Plus Regeneration Hair Care which is product labeled by Ecobio Medical Institute, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70937-100-02 1 kit in 1 package * 3 ampule in 1 package (70937-102-02) / 10 ml in 1 ampule (70937-102-01) * 1 bottle in 1 package (70937-103-02) / 120 ml in 1 bottle (70937-103-01) * 1 bottle in 1 package (70937-101-02) / 200 ml in 1 bottle (70937-101-01). 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 Eh Hair Plus Regeneration Hair Care?

Hair cool shampoo - Wet hair with lukewarm water and pump 2-4 times and apply on scalp and hair evenly. Massage gently and rinse clean.Hair stick aroma ampoule- Roll over scalp evenly from the center when it is needed.Hair tonic- Shake well, apply on scalp evenly every day and massage gently with fingertips until it is absorbed enough. Dry hair.

Which are Eh Hair Plus Regeneration Hair Care UNII Codes?

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

Which are Eh Hair Plus Regeneration Hair Care 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".