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  4. NDC Product Code: 72667-006 Dg Health

NDC 72667-006 Dg Health

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72667-006?
  4. Dg Health 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:
72667-006
Proprietary Name:
Dg Health
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Inspec Solutions Llc.
Labeler Code:
72667
Product Label ID:
7cd6b829-3500-60dd-e053-2991aa0aad12
Start Marketing Date: [9]
01-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 72667-006?

The NDC code 72667-006 is assigned by the FDA to the product Dg Health which is product labeled by Inspec Solutions Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72667-006-01 148 ml in 1 bottle, spray . 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 Dg Health?

Usesfirst aid to help prevent bacterial contamination or skin infection, and for temporary relief of pain and itching associated with minor: cute, scrapes, burns, sunburn, skin irritations

Which are Dg Health UNII Codes?

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

Which are Dg Health 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 Dg Health?

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:
  • RxCUI: 1012099 - benzalkonium Cl 0.13 % / lidocaine HCl 2.5 % Topical Spray
  • RxCUI: 1012099 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 25 MG/ML Topical Spray

* 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".