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  4. NDC Product Code: 73111-0001 Guerison All In One Tocx

NDC 73111-0001 Guerison All In One Tocx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73111-0001?
  4. Guerison All In One Tocx 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:
73111-0001
Proprietary Name:
Guerison All In One Tocx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guerison Green Global Company Limited
Labeler Code:
73111
Product Label ID:
889329b8-2b29-7217-e053-2a95a90ad825
Start Marketing Date: [9]
05-11-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73111-0001?

The NDC code 73111-0001 is assigned by the FDA to the product Guerison All In One Tocx which is product labeled by Guerison Green Global Company Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73111-0001-1 120 ml in 1 bottle . 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 Guerison All In One Tocx?

After using skin lotion, apply and spread an appropriate amount evenly over the entire facewhen a bubble is generated, tap it gently to be absorbed into your skin

Which are Guerison All In One Tocx UNII Codes?

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

Which are Guerison All In One Tocx 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".