NDC 73946-002 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:
73946-002
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yiwu Jiefei Daily Chemicals Co.,ltd.
Labeler Code:
73946
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 73946-002-01

Package Description: 24 CONTAINER in 1 CARTON / 2 BOTTLE in 1 CONTAINER / 60 mL in 1 BOTTLE

NDC Code 73946-002-02

Package Description: 96 BOX in 1 CARTON / 24 CONTAINER in 1 BOX / 2 BOTTLE in 1 CONTAINER / 10 mL in 1 BOTTLE

NDC Code 73946-002-03

Package Description: 96 BOX in 1 CARTON / 24 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE

NDC Code 73946-002-04

Package Description: 24 CONTAINER in 1 CARTON / 2 BOTTLE in 1 CONTAINER / 50 mL in 1 BOTTLE

NDC Code 73946-002-05

Package Description: 24 BOTTLE in 1 CARTON / 237 mL in 1 BOTTLE

NDC Code 73946-002-06

Package Description: 24 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE

NDC Code 73946-002-07

Package Description: 72 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE

NDC Code 73946-002-08

Package Description: 12 BOTTLE in 1 CARTON / 1000 mL in 1 BOTTLE

Product Details

What is NDC 73946-002?

The NDC code 73946-002 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Yiwu Jiefei Daily Chemicals Co.,ltd.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 73946-002-01 24 container in 1 carton / 2 bottle in 1 container / 60 ml in 1 bottle, 73946-002-02 96 box in 1 carton / 24 container in 1 box / 2 bottle in 1 container / 10 ml in 1 bottle, 73946-002-03 96 box in 1 carton / 24 bottle in 1 box / 30 ml in 1 bottle, 73946-002-04 24 container in 1 carton / 2 bottle in 1 container / 50 ml in 1 bottle, 73946-002-05 24 bottle in 1 carton / 237 ml in 1 bottle, 73946-002-06 24 bottle in 1 carton / 500 ml in 1 bottle, 73946-002-07 72 bottle in 1 carton / 100 ml in 1 bottle, 73946-002-08 12 bottle in 1 carton / 1000 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 Hand Sanitizer?

Directions: Wet hands thoroughly and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Which are Hand Sanitizer UNII Codes?

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

Which are 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 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".