NDC 50353-100 Purmist

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:
50353-100
Proprietary Name:
Purmist
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mkr International Inc
Labeler Code:
50353
Start Marketing Date: [9]
06-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50353-100-10

Package Description: 1 BOTTLE, PUMP in 1 BLISTER PACK / 7.1 mL in 1 BOTTLE, PUMP

NDC Code 50353-100-20

Package Description: 6 BAG in 1 CARTON / 400 mL in 1 BAG

NDC Code 50353-100-50

Package Description: 6 BOTTLE, SPRAY in 1 CARTON / 100 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 50353-100?

The NDC code 50353-100 is assigned by the FDA to the product Purmist which is product labeled by Mkr International Inc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 50353-100-10 1 bottle, pump in 1 blister pack / 7.1 ml in 1 bottle, pump, 50353-100-20 6 bag in 1 carton / 400 ml in 1 bag, 50353-100-50 6 bottle, spray in 1 carton / 100 ml in 1 bottle, spray. 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.

Which are Purmist UNII Codes?

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

Which are Purmist 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:

What is the NDC to RxNorm Crosswalk for Purmist?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1049648 - ethanol 70 % / chlorhexidine gluconate 1 % Topical Solution
  • RxCUI: 1049648 - chlorhexidine gluconate 10 MG/ML / ethanol 0.7 ML/ML Topical Solution
  • RxCUI: 1049648 - chlorhexidine gluconate 1 % / ethanol 70 % Topical Solution

* 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".