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  4. NDC Product Code: 79002-162 Relief Hand Sanitizing Wipes

NDC 79002-162 Relief Hand Sanitizing Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79002-162?
  4. Relief Hand Sanitizing Wipes 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:
79002-162
Proprietary Name:
Relief Hand Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Daehan P&h Co., Ltd.
Labeler Code:
79002
Product Label ID:
a8aba3bd-55b6-14d1-e053-2995a90a2a0f
Start Marketing Date: [9]
06-22-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79002-162?

The NDC code 79002-162 is assigned by the FDA to the product Relief Hand Sanitizing Wipes which is product labeled by Daehan P&h Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79002-162-20 20 packet in 1 box / 1 cloth in 1 packet (79002-162-01). 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 Relief Hand Sanitizing Wipes?

■ Remove the wipes one by one, and use on the skin gently. ■ There is a risk of contamination if the wet wipe is put back into the packaging with unclean hands. ■ Do not throw away wipes in a flush toilet, as there is a risk of clogging it. ■ Supervise children under 6 years of age when using. ■ Do not allow infants and toddlers swallow or put in the mouth. ■ Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.) ■ Keep product in its original container as storing the product in anything other than the original container may result in accidents or cause the integrity of the product to diminish.

Which are Relief Hand Sanitizing Wipes UNII Codes?

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

Which are Relief Hand Sanitizing Wipes 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".