Tongyi Cleanguard 84 Disinfectant
NDC 73681-1001
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
Tongyi Cleanguard 84 Disinfectant is a UNAPPROVED DRUG OTHER-approved product labeled by Tongyi Petroleum Chemical Co., Ltd.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 73681-1001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
73681-1001
Proprietary Name:
Tongyi Cleanguard 84 Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
73681
Product Label ID:
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Marketing Timeline
Start Marketing Date: [9]
03-11-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Product Characteristics
Shape:
FREEFORM (C48340)
Code Structure Chart
Product Details
What is NDC 73681-1001?
The NDC code 73681-1001 is assigned by the FDA to the product Tongyi Cleanguard 84 Disinfectant. This pharmaceutical product is labeled by Tongyi Petroleum Chemical Co., Ltd. and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 73681-1001-3. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
1, For disinfection of general object surfaces, dilute this product with water at a ratio of 1:100 to prepare a diluent with sodium hypochlorite content of 400mg/L, wipe it with the diluent for 20 minutes.
2, For disinfection of contaminated object surfaces of infectious patients, dilute this product with water at a ratio of 1:6.5 to prepare a diluent with sodium hypochlorite content of 6000mg/L, soak it in the diluent for 60 minutes.
3, For disinfectant of fruits and vegetables, dilute this product with water at a ration of 1:400 to prepare a diluent with sodium hypochlorite content of 100mg/L, soak it in the diluent for 10 minutes and rinse with clean water.
4, For disinfection of the tableware, dilute this product with water at a ratio of 1:100 to prepare a diluent with sodium hypochlorite content of 400mg/L, soak it with the diluent for 20 minutes and rinse with clean water.
5, For disinfection of the fabric, dilute this product with water at a ratio of 1:100 to prepare a diluent with sodium hypochlorite content of 400mg/L, soak it with the diluent for 20 minutes and rinse with clean water.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
- HYPOCHLORITE ION (UNII: T5UM7HB19N) (Active Moiety)
Which are the Inactive Ingredients associated 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:
- WATER (UNII: 059QF0KO0R)
* Please review the full disclaimer at the bottom of this page.
Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
