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  4. NDC Product Code: 67313-9200 Merfin Mates Hand Sanitizing Towels

NDC 67313-9200 Merfin Mates Hand Sanitizing Towels

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67313-9200?
  5. Merfin Mates Hand Sanitizing Towels 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:
67313-9200
Proprietary Name:
Merfin Mates Hand Sanitizing Towels
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nps Holdings Llc
Labeler Code:
67313
Product Label ID:
a75aa40a-c6d6-560f-e053-2a95a90ae534
Start Marketing Date: [9]
05-13-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLOTH)
Shape:
RECTANGLE (C48347)

Code Structure Chart

Product Details

What is NDC 67313-9200?

The NDC code 67313-9200 is assigned by the FDA to the product Merfin Mates Hand Sanitizing Towels which is product labeled by Nps Holdings Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67313-9200-0 1 cloth in 1 bag . 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 Merfin Mates Hand Sanitizing Towels?

This product is intended for use in:Hospitals and healthcare centersSchools and daycaresNursing homesGrocery storesGyms and fitness clubsAirports and stadiumsVeterinary clinics and kennelsBeauty salons and barber shops

Which are Merfin Mates Hand Sanitizing Towels UNII Codes?

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

Which are Merfin Mates Hand Sanitizing Towels 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".