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NDC 81752-010 Everytoktok Hair Tonic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81752-010?
  4. Everytoktok Hair Tonic 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:
81752-010
Proprietary Name:
Everytoktok Hair Tonic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dreamin
Labeler Code:
81752
Product Label ID:
459805a4-ad70-43e6-aa3f-75bedd9619cb
Start Marketing Date: [9]
03-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81752-010?

The NDC code 81752-010 is assigned by the FDA to the product Everytoktok Hair Tonic which is product labeled by Dreamin. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81752-010-02 1 bottle in 1 carton / 120 ml in 1 bottle (81752-010-01). 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 Everytoktok Hair Tonic?

■ For the first use, strongly tap the silicon brush on the back of the hand until the solution is ejected. When the solution starts to come out, tap it lightly on the scalp to use.

Which are Everytoktok Hair Tonic UNII Codes?

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

Which are Everytoktok 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:

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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".