79519-020 NDC - JANITEX ()

Drug Information

Product NDC: 79519-020

Proprietary Name: JANITEX

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Pacific Health Systems Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/30/2020

Package Information

No. Package Code Package Description Billing Unit
179519-020-0180 PACKAGE in 1 CANISTER (79519-020-01) / 4.16 mL in 1 PACKAGE
279519-020-0260 PACKAGE in 1 BOX (79519-020-02) / 4.16 mL in 1 PACKAGE
379519-020-0340 PACKAGE in 1 PACKET (79519-020-03) / 4.16 mL in 1 PACKAGE
479519-020-0480 PACKAGE in 1 CANISTER (79519-020-04) / 4.16 mL in 1 PACKAGE

NDC Record

Field Name Field Value Definition
PRODUCT NDC79519-020The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEJANITEXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX75% ALCOHOL WET WIPESA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE6/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPacific Health Systems Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023