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  4. NDC Product Code: 77022-1114 Ehs7000-4

NDC 77022-1114 Ehs7000-4

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 77022-1114?
  5. Ehs7000-4 Uses
  6. Active Ingredients UNII Codes
  7. 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:
77022-1114
Proprietary Name:
Ehs7000-4
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Epic Chemistry Llc
Labeler Code:
77022
Product Label ID:
af9a64b7-d38f-6822-e053-2995a90aecbd
Start Marketing Date: [9]
09-07-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 77022-1114-4

Package Description: 1 GEL in 1 BOTTLE

Product Details

What is NDC 77022-1114?

The NDC code 77022-1114 is assigned by the FDA to the product Ehs7000-4 which is product labeled by Epic Chemistry Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77022-1114-4 1 gel 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 Ehs7000-4?

Place a generous amount of product on hands and rub hands together until dry.

Which are Ehs7000-4 UNII Codes?

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

Which are Ehs7000-4 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".