1. Home
  2. Labeler Index
  3. Prime Pace Products Llc
  4. NDC Product Code: 79183-301 Seren Guard Sanitizing Wipes

NDC 79183-301 Seren Guard Sanitizing Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79183-301?
  4. Seren Guard 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:
79183-301
Proprietary Name:
Seren Guard Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prime Pace Products Llc
Labeler Code:
79183
Product Label ID:
5a17a844-cccf-430f-8223-59795566f0a5
Start Marketing Date: [9]
07-13-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79183-301?

The NDC code 79183-301 is assigned by the FDA to the product Seren Guard Sanitizing Wipes which is product labeled by Prime Pace Products Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 79183-301-08 80 patch in 1 bottle, dispensing , 79183-301-16 160 patch in 1 bottle, dispensing , 79183-301-20 200 patch in 1 bottle, dispensing . 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 Seren Guard Sanitizing Wipes?

■ Thoroughly wipe hands as desired.■ Allow to dry without wiping.■ Discard wipe after use.■ Do not flush.

Which are Seren Guard Sanitizing Wipes UNII Codes?

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

Which are Seren Guard 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:

* 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".