NDC 75239-005 Advance 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:
75239-005
Proprietary Name:
Advance Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Youxing Cosmetics Co.,ltd
Labeler Code:
75239
Start Marketing Date: [9]
04-21-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Product Packages

NDC Code 75239-005-01

Package Description: 30 mL in 1 BOTTLE

NDC Code 75239-005-02

Package Description: 50 mL in 1 BOTTLE

NDC Code 75239-005-03

Package Description: 80 mL in 1 BOTTLE

NDC Code 75239-005-04

Package Description: 100 mL in 1 BOTTLE

NDC Code 75239-005-05

Package Description: 120 mL in 1 BOTTLE

NDC Code 75239-005-06

Package Description: 150 mL in 1 BOTTLE

NDC Code 75239-005-07

Package Description: 180 mL in 1 BOTTLE

NDC Code 75239-005-08

Package Description: 200 mL in 1 BOTTLE

NDC Code 75239-005-09

Package Description: 240 mL in 1 BOTTLE

NDC Code 75239-005-10

Package Description: 250 mL in 1 BOTTLE

NDC Code 75239-005-11

Package Description: 300 mL in 1 BOTTLE

NDC Code 75239-005-12

Package Description: 350 mL in 1 BOTTLE

NDC Code 75239-005-13

Package Description: 500 mL in 1 BOTTLE

NDC Code 75239-005-14

Package Description: 650 mL in 1 BOTTLE

NDC Code 75239-005-15

Package Description: 1000 mL in 1 BOTTLE

NDC Code 75239-005-16

Package Description: 3800 mL in 1 BOTTLE

NDC Code 75239-005-17

Package Description: 5000 mL in 1 BOTTLE

NDC Code 75239-005-18

Package Description: 20000 mL in 1 BOTTLE

NDC Code 75239-005-19

Package Description: 50000 mL in 1 BOTTLE

NDC Code 75239-005-20

Package Description: 1000000 mL in 1 BOTTLE

Product Details

What is NDC 75239-005?

The NDC code 75239-005 is assigned by the FDA to the product Advance Hand Sanitizer which is product labeled by Guangzhou Youxing Cosmetics Co.,ltd. The product's dosage form is . The product is distributed in 20 packages with assigned NDC codes 75239-005-01 30 ml in 1 bottle , 75239-005-02 50 ml in 1 bottle , 75239-005-03 80 ml in 1 bottle , 75239-005-04 100 ml in 1 bottle , 75239-005-05 120 ml in 1 bottle , 75239-005-06 150 ml in 1 bottle , 75239-005-07 180 ml in 1 bottle , 75239-005-08 200 ml in 1 bottle , 75239-005-09 240 ml in 1 bottle , 75239-005-10 250 ml in 1 bottle , 75239-005-11 300 ml in 1 bottle , 75239-005-12 350 ml in 1 bottle , 75239-005-13 500 ml in 1 bottle , 75239-005-14 650 ml in 1 bottle , 75239-005-15 1000 ml in 1 bottle , 75239-005-16 3800 ml in 1 bottle , 75239-005-17 5000 ml in 1 bottle , 75239-005-18 20000 ml in 1 bottle , 75239-005-19 50000 ml in 1 bottle , 75239-005-20 1000000 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 Advance Hand Sanitizer?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Advance Hand Sanitizer UNII Codes?

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

Which are Advance 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 Advance 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".