1. Home
  2. Labeler Index
  3. Dong Hiep Trading And Investment Co., Ltd
  4. NDC Product Code: 79366-103 Battle Skin Alcohol Wipes

NDC 79366-103 Battle Skin Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79366-103?
  4. Battle Skin Alcohol 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:
79366-103
Proprietary Name:
Battle Skin Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dong Hiep Trading And Investment Co., Ltd
Labeler Code:
79366
Product Label ID:
aa5f4aca-c149-741d-e053-2a95a90a803a
Start Marketing Date: [9]
07-14-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79366-103?

The NDC code 79366-103 is assigned by the FDA to the product Battle Skin Alcohol Wipes which is product labeled by Dong Hiep Trading And Investment Co., Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 79366-103-50 260 g in 1 pouch , 79366-103-99 520 g in 1 pouch . 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 Battle Skin Alcohol Wipes?

Used for antibacterial hand skin.

Which are Battle Skin Alcohol Wipes UNII Codes?

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

Which are Battle Skin Alcohol 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:

* 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".