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  4. NDC Product Code: 81799-005 Herpes Relief Cream

NDC 81799-005 Herpes Relief Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81799-005?
  4. Herpes Relief Cream 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 certification is expired.
NDC Product Code:
81799-005
Proprietary Name:
Herpes Relief Cream
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Ehy Holdings Llc
Labeler Code:
81799
Product Label ID:
f209ee77-d290-1203-e053-2a95a90adb8c
Start Marketing Date: [9]
01-11-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 81799-005?

The NDC code 81799-005 is assigned by the FDA to the product Herpes Relief Cream which is product labeled by Ehy Holdings Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81799-005-01 60 g 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 Herpes Relief Cream?

Adult and children over 12 vears or old. Wash handsbefore and after applying the cream. Apply to affected area at the firstsign of blisters, sores, or tingling sensation. Rub in gently andthoroughly. Do not use more than 3 times daily. Children under 12years: ask a docto

Which are Herpes Relief Cream UNII Codes?

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

Which are Herpes Relief Cream 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".