NDC 82358-0001 Dr. Guard Stick

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:
82358-0001
Proprietary Name:
Dr. Guard Stick
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jbk Forms Co Ltd
Labeler Code:
82358
Start Marketing Date: [9]
11-04-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82358-0001-1

Package Description: 10 g in 1 CONTAINER

Product Details

What is NDC 82358-0001?

The NDC code 82358-0001 is assigned by the FDA to the product Dr. Guard Stick which is product labeled by Jbk Forms Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82358-0001-1 10 g in 1 container . 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 Dr. Guard Stick?

How to Use (How to Activate) - The stick contains a main liquid solution and an ampoule inside that includes active ingredients in powder form. Bend the middle part of the stick to break the ampoule. Once the ampoule inside the stick cracks, sufficiently shake the stick to mix the powder with the solution well. As it turns yellow, the stick is activated and the pure chlorine dioxide is released through the surface of the stick. After 3~4 weeks of usage, the stick will turn transparent which indicates that it is no longer effective. Please dispose the used stick into a general trash bag.

Which are Dr. Guard Stick UNII Codes?

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

Which are Dr. Guard Stick 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:

* 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".