NDC 54125-008 Disinfectant Solution

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:
54125-008
Proprietary Name:
Disinfectant Solution
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
54125
Start Marketing Date: [9]
04-25-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
ECOFINEST

Code Structure Chart

Product Details

What is NDC 54125-008?

The NDC code 54125-008 is assigned by the FDA to the product Disinfectant Solution which is product labeled by Shanghai Rijie Environmental Technology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54125-008-01 60 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 Disinfectant Solution?

after clearing the source of pollutants, close doors and windows, use sprayer to spray the product at the dosage of 5mL/m' with the sprayer head in the air, evenly from top to bottom, lcft to right.Open doors and windows after taking efective for 30 minutes.Disinfection of food processing appliances (tableware) and equipment: after clearing the pollutants, spray and wipe the surface of the object to be disinfected with the original solution, taking effective for 5 minutes

Which are Disinfectant Solution UNII Codes?

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

Which are Disinfectant Solution 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".