1. Home
  2. Labeler Index
  3. Foshan Eric Biotechnology Co., Ltd.
  4. NDC Product Code: 41768-001 Alkaline Super Ionized Water

NDC 41768-001 Alkaline Super Ionized Water

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41768-001?
  4. Alkaline Super Ionized Water 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:
41768-001
Proprietary Name:
Alkaline Super Ionized Water
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Foshan Eric Biotechnology Co., Ltd.
Labeler Code:
41768
Product Label ID:
a79dd0bd-9f93-70cf-e053-2a95a90a8366
Start Marketing Date: [9]
06-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 41768-001?

The NDC code 41768-001 is assigned by the FDA to the product Alkaline Super Ionized Water which is product labeled by Foshan Eric Biotechnology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41768-001-01 100 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 Alkaline Super Ionized Water?

①Spray directly on the surface of the object and dry it or let dry naturally.②dip the product with a paper towel and let dry naturally.③spray directly on the surface of the food and rinse with water.

Which are Alkaline Super Ionized Water UNII Codes?

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

Which are Alkaline Super Ionized Water 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".