NDC 42961-159 Thesafetydirector Aquapreserv

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42961-159
Proprietary Name:
Thesafetydirector Aquapreserv
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cintas Corporation
Labeler Code:
42961
Start Marketing Date: [9]
07-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42961-159-01

Package Description: 947 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 42961-159?

The NDC code 42961-159 is assigned by the FDA to the product Thesafetydirector Aquapreserv which is product labeled by Cintas Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42961-159-01 947 ml in 1 bottle, plastic . 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 Thesafetydirector Aquapreserv?

•concentrate must be diluted•wear protective eyewear, and gloves•clean portable self-contained station•rinse with potable water•partially fill station (approximately 2-3 gallons) with potable water•add entire contents of this bottle•agitate or mix thoroughly•fill station to mark•date station’s inspection tag•change station solution at least every 120-180 days, or when eyewash station is use•use good judgment based upon the station’s environmental exposure to determine when scheduled solution changes should occur•in advance of an emergency

Which are Thesafetydirector Aquapreserv UNII Codes?

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

Which are Thesafetydirector Aquapreserv 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".