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NDC 0924-0169 Physicianscare Eyewash Station Additive Concentrate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0924-0169?
  4. Physicianscare Eyewash Station Additive Concentrate 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:
0924-0169
Proprietary Name:
Physicianscare Eyewash Station Additive Concentrate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Acme United Corporation
Labeler Code:
0924
Product Label ID:
2a3f0a3e-3ae2-4d7e-e054-00144ff88e88
Start Marketing Date: [9]
01-26-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 0924-0169?

The NDC code 0924-0169 is assigned by the FDA to the product Physicianscare Eyewash Station Additive Concentrate which is product labeled by Acme United Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0924-0169-08 .236 l in 1 bottle, unit-dose . 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 Physicianscare Eyewash Station Additive Concentrate?

UseA preservative for use in potable self-contained emergency eyewash stations

Which are Physicianscare Eyewash Station Additive Concentrate UNII Codes?

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

Which are Physicianscare Eyewash Station Additive Concentrate 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".