NDC 79762-001 Dfenze Hocl Sanitizer And Disinfectant

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:
79762-001
Proprietary Name:
Dfenze Hocl Sanitizer And Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
79762
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 79762-001?

The NDC code 79762-001 is assigned by the FDA to the product Dfenze Hocl Sanitizer And Disinfectant which is product labeled by Jl Water Engineering Sdn. Bhd.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 79762-001-01 30 ml in 1 bottle , 79762-001-02 50 ml in 1 bottle , 79762-001-03 100 ml in 1 bottle , 79762-001-04 500 ml in 1 bottle , 79762-001-05 2000 ml in 1 bottle , 79762-001-06 5000 ml in 1 bottle , 79762-001-07 10000 ml in 1 bottle , 79762-001-08 20000 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 Dfenze Hocl Sanitizer And Disinfectant?

1. Turn the spray cap ON 2. Shake lightly and spray with 20cm distance for 3-5 times from the object 3. Dry the object well after spraying 4. Clean the application site if required. 5. Turn the spray cap OFF after use. Repeat as needed throughout the day. Use it for your daily regimen. No rinsing required.

Which are Dfenze Hocl Sanitizer And Disinfectant UNII Codes?

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

Which are Dfenze Hocl Sanitizer And Disinfectant 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".