NDC 78852-000 Si Master Hand Sanitizer

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:
78852-000
Proprietary Name:
Si Master Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
78852
Start Marketing Date: [9]
06-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 78852-000?

The NDC code 78852-000 is assigned by the FDA to the product Si Master Hand Sanitizer which is product labeled by Ningbo Youcheng Trade Developing Co., Ltd.. The product's dosage form is . The product is distributed in 53 packages with assigned NDC codes 78852-000-01 30 ml in 1 tube , 78852-000-02 60 ml in 1 tube , 78852-000-03 80 ml in 1 tube , 78852-000-04 100 ml in 1 tube , 78852-000-05 120 ml in 1 tube , 78852-000-06 150 ml in 1 tube , 78852-000-07 160 ml in 1 tube , 78852-000-08 180 ml in 1 tube , 78852-000-09 200 ml in 1 tube , 78852-000-10 30 ml in 1 bottle , 78852-000-11 60 ml in 1 bottle , 78852-000-12 100 ml in 1 bottle , 78852-000-13 237 ml in 1 bottle , 78852-000-14 300 ml in 1 bottle , 78852-000-15 400 ml in 1 bottle , 78852-000-16 500 ml in 1 bottle , 78852-000-17 750 ml in 1 bottle , 78852-000-18 1000 ml in 1 bottle , 78852-000-19 30 ml in 1 bottle, pump , 78852-000-20 60 ml in 1 bottle, pump , 78852-000-21 100 ml in 1 bottle, pump , 78852-000-22 237 ml in 1 bottle, pump , 78852-000-23 300 ml in 1 bottle, pump , 78852-000-24 400 ml in 1 bottle, pump , 78852-000-25 500 ml in 1 bottle, pump , 78852-000-26 750 ml in 1 bottle, pump , 78852-000-27 1000 ml in 1 bottle, pump , 78852-000-28 250 ml in 1 bottle, plastic , 78852-000-29 300 ml in 1 bottle, plastic , 78852-000-30 500 ml in 1 bottle, plastic , 78852-000-31 1000 ml in 1 bottle, plastic , 78852-000-32 2000 ml in 1 bottle, plastic , 78852-000-33 2500 ml in 1 bottle, plastic , 78852-000-34 3000 ml in 1 bottle, plastic , 78852-000-35 3500 ml in 1 bottle, plastic , 78852-000-36 4000 ml in 1 bottle, plastic , 78852-000-37 4500 ml in 1 bottle, plastic , 78852-000-38 5000 ml in 1 bottle, plastic , 78852-000-39 6000 ml in 1 bottle, plastic , 78852-000-40 10000 ml in 1 bottle, plastic , 78852-000-41 250 ml in 1 bottle, pump , 78852-000-42 1000 ml in 1 bottle, pump , 78852-000-43 2000 ml in 1 bottle, pump , 78852-000-44 2500 ml in 1 bottle, pump , 78852-000-45 3000 ml in 1 bottle, pump , 78852-000-46 3500 ml in 1 bottle, pump , 78852-000-47 4000 ml in 1 bottle, pump , 78852-000-48 4500 ml in 1 bottle, pump , 78852-000-49 5000 ml in 1 bottle, pump , 78852-000-50 6000 ml in 1 bottle, pump , 78852-000-51 10000 ml in 1 bottle, pump , 78852-000-52 300 ml in 1 bottle, pump , 78852-000-53 500 ml in 1 bottle, pump . 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 Si Master Hand Sanitizer?

This product is used as Antiseptic

Which are Si Master Hand Sanitizer UNII Codes?

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

Which are Si Master Hand Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Si Master Hand Sanitizer?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".