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  4. NDC Product Code: 71638-0004 Biotoc Regen Peel

NDC 71638-0004 Biotoc Regen Peel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71638-0004?
  4. Biotoc Regen Peel 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:
71638-0004
Proprietary Name:
Biotoc Regen Peel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermafirm Inc.
Labeler Code:
71638
Product Label ID:
58554a7e-90cd-f2da-e053-2991aa0af4dc
Start Marketing Date: [9]
09-04-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 71638-0004?

The NDC code 71638-0004 is assigned by the FDA to the product Biotoc Regen Peel which is product labeled by Dermafirm Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71638-0004-1 13.5 g in 1 bottle, with applicator . 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 Biotoc Regen Peel?

Apply an appropriate amount of BIOTOC Regen Peel to pores and wrinkles especially around the lips and under the eyes.Then massage roundly with your fingertips pressure for 2 or 3 minutes, and press firmly with your fingers. Apply BIOTOC Serum and Cream thickly after using BIOTOC Regen Peel.It is effective to use mask pack together. For the best results, apply BIOTOC Regen Peel twice a week and BIOTOC Regen Ampoule, Serum, and Cream every morning and evening.

Which are Biotoc Regen Peel UNII Codes?

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

Which are Biotoc Regen Peel 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".