NDC 49589-199 Periactive

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:
49589-199
Proprietary Name:
Periactive
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Izun Pharmaceuticals Corp
Labeler Code:
49589
Start Marketing Date: [9]
02-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49589-199-10

Package Description: 100 mL in 1 BOTTLE

NDC Code 49589-199-50

Package Description: 12 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE

Product Details

What is NDC 49589-199?

The NDC code 49589-199 is assigned by the FDA to the product Periactive which is product labeled by Izun Pharmaceuticals Corp. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49589-199-10 100 ml in 1 bottle , 49589-199-50 12 bottle in 1 carton / 500 ml in 1 bottle. 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 Periactive?

Adults and children 12 years and olderrinse for 60 seconds with 15ml (3 teaspoonful) twice a daychildren 6-12 yearsrinse for 60 seconds with 10ml (2 teaspoonful) twice a daychildren under 6 years of agedo not usedo not eat, drink or rinse your mouth for 30 minutes after usedo not swallowchildren 6 years to under 12 years of age: supervise use

Which are Periactive UNII Codes?

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

Which are Periactive 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".