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NDC 67151-313 Benzalkonium Chloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67151-313?
  4. Benzalkonium Chloride 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:
67151-313
Proprietary Name:
Benzalkonium Chloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Progressive
Labeler Code:
67151
Product Label ID:
db0c6220-34f5-3fb0-e053-2a95a90a85af
Start Marketing Date: [9]
03-29-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 67151-313?

The NDC code 67151-313 is assigned by the FDA to the product Benzalkonium Chloride which is product labeled by Progressive. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 67151-313-04 240 canister in 1 canister / 1 mg in 1 canister, 67151-313-09 1500 canister in 1 canister / 1 mg in 1 canister. 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 Benzalkonium Chloride?

Remove lidPull wipe from center of roll and thread through opening in lidDo not push finger through openingReplace lid, pull wipe up, and then out 45° angleThe next wipe dispenses automaticallyClose lid to retain moisture

Which are Benzalkonium Chloride UNII Codes?

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

Which are Benzalkonium Chloride 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".