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  4. NDC Product Code: 72316-001 Active Hydrogen Professional

NDC 72316-001 Active Hydrogen Professional

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72316-001?
  4. Active Hydrogen Professional Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72316-001
Proprietary Name:
Active Hydrogen Professional
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Executive Pro Solutions Doo
Labeler Code:
72316
Product Label ID:
80bcc187-15b2-40b0-b338-8cfb2c2b813b
Start Marketing Date: [9]
05-11-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72316-001-01

Package Description: 100 mL in 1 TUBE

Product Details

What is NDC 72316-001?

The NDC code 72316-001 is assigned by the FDA to the product Active Hydrogen Professional which is product labeled by Executive Pro Solutions Doo. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72316-001-01 100 ml in 1 tube . 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 Active Hydrogen Professional?

This product is used as External analgesic. Reduces and stops the inflammatory process, eliminates pain, reduces swelling, speeds uprecovery process after injuries, neutralizes excretion of lactic acid in the muscles

Which are Active Hydrogen Professional UNII Codes?

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

Which are Active Hydrogen Professional 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:

What is the NDC to RxNorm Crosswalk for Active Hydrogen Professional?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".