NDC 73905-007 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.

Product Packages

NDC Code 73905-007-01

Package Description: 2 mL in 1 BOTTLE

NDC Code 73905-007-02

Package Description: 5 mL in 1 BOTTLE

NDC Code 73905-007-03

Package Description: 10 mL in 1 BOTTLE

NDC Code 73905-007-04

Package Description: 20 mL in 1 BOTTLE

NDC Code 73905-007-05

Package Description: 30 mL in 1 BOTTLE

NDC Code 73905-007-06

Package Description: 45 mL in 1 BOTTLE

NDC Code 73905-007-07

Package Description: 55 mL in 1 BOTTLE

NDC Code 73905-007-08

Package Description: 60 mL in 1 BOTTLE

NDC Code 73905-007-09

Package Description: 80 mL in 1 BOTTLE

NDC Code 73905-007-10

Package Description: 100 mL in 1 BOTTLE

NDC Code 73905-007-11

Package Description: 120 mL in 1 BOTTLE

NDC Code 73905-007-12

Package Description: 180 mL in 1 BOTTLE

NDC Code 73905-007-13

Package Description: 200 mL in 1 BOTTLE

NDC Code 73905-007-14

Package Description: 236 mL in 1 BOTTLE

NDC Code 73905-007-15

Package Description: 237 mL in 1 BOTTLE

NDC Code 73905-007-16

Package Description: 240 mL in 1 BOTTLE

NDC Code 73905-007-17

Package Description: 250 mL in 1 BOTTLE

NDC Code 73905-007-18

Package Description: 260 mL in 1 BOTTLE

NDC Code 73905-007-19

Package Description: 300 mL in 1 BOTTLE

NDC Code 73905-007-20

Package Description: 350 mL in 1 BOTTLE

NDC Code 73905-007-21

Package Description: 400 mL in 1 BOTTLE

NDC Code 73905-007-22

Package Description: 500 mL in 1 BOTTLE

NDC Code 73905-007-23

Package Description: 560 mL in 1 BOTTLE

NDC Code 73905-007-24

Package Description: 600 mL in 1 BOTTLE

NDC Code 73905-007-25

Package Description: 750 mL in 1 BOTTLE

NDC Code 73905-007-26

Package Description: 900 mL in 1 BOTTLE

NDC Code 73905-007-27

Package Description: 980 mL in 1 BOTTLE

NDC Code 73905-007-28

Package Description: 985 mL in 1 BOTTLE

NDC Code 73905-007-29

Package Description: 1000 mL in 1 BOTTLE

NDC Code 73905-007-30

Package Description: 1300 mL in 1 BOTTLE

NDC Code 73905-007-31

Package Description: 1500 mL in 1 BOTTLE

NDC Code 73905-007-32

Package Description: 1800 mL in 1 BOTTLE

NDC Code 73905-007-33

Package Description: 2000 mL in 1 BOTTLE

NDC Code 73905-007-34

Package Description: 2500 mL in 1 BOTTLE

NDC Code 73905-007-35

Package Description: 3000 mL in 1 BOTTLE

NDC Code 73905-007-36

Package Description: 3800 mL in 1 BOTTLE

NDC Code 73905-007-37

Package Description: 4000 mL in 1 BOTTLE

NDC Code 73905-007-38

Package Description: 5000 mL in 1 BOTTLE

NDC Code 73905-007-39

Package Description: 10000 mL in 1 BOTTLE

NDC Code 73905-007-40

Package Description: 20000 mL in 1 BOTTLE

NDC Code 73905-007-41

Package Description: 25000 mL in 1 BOTTLE

NDC Code 73905-007-42

Package Description: 45000 mL in 1 BOTTLE

NDC Code 73905-007-43

Package Description: 50000 mL in 1 BOTTLE

NDC Code 73905-007-44

Package Description: 100000 mL in 1 BOTTLE

NDC Code 73905-007-45

Package Description: 200000 mL in 1 BOTTLE

NDC Code 73905-007-46

Package Description: 500000 mL in 1 BOTTLE

NDC Code 73905-007-47

Package Description: 1000000 mL in 1 BOTTLE

Product Details

What is NDC 73905-007?

The NDC code 73905-007 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Zhejiang Jinghui Cosmetics Share Co.,ltd. The product's dosage form is . The product is distributed in 47 packages with assigned NDC codes 73905-007-01 2 ml in 1 bottle , 73905-007-02 5 ml in 1 bottle , 73905-007-03 10 ml in 1 bottle , 73905-007-04 20 ml in 1 bottle , 73905-007-05 30 ml in 1 bottle , 73905-007-06 45 ml in 1 bottle , 73905-007-07 55 ml in 1 bottle , 73905-007-08 60 ml in 1 bottle , 73905-007-09 80 ml in 1 bottle , 73905-007-10 100 ml in 1 bottle , 73905-007-11 120 ml in 1 bottle , 73905-007-12 180 ml in 1 bottle , 73905-007-13 200 ml in 1 bottle , 73905-007-14 236 ml in 1 bottle , 73905-007-15 237 ml in 1 bottle , 73905-007-16 240 ml in 1 bottle , 73905-007-17 250 ml in 1 bottle , 73905-007-18 260 ml in 1 bottle , 73905-007-19 300 ml in 1 bottle , 73905-007-20 350 ml in 1 bottle , 73905-007-21 400 ml in 1 bottle , 73905-007-22 500 ml in 1 bottle , 73905-007-23 560 ml in 1 bottle , 73905-007-24 600 ml in 1 bottle , 73905-007-25 750 ml in 1 bottle , 73905-007-26 900 ml in 1 bottle , 73905-007-27 980 ml in 1 bottle , 73905-007-28 985 ml in 1 bottle , 73905-007-29 1000 ml in 1 bottle , 73905-007-30 1300 ml in 1 bottle , 73905-007-31 1500 ml in 1 bottle , 73905-007-32 1800 ml in 1 bottle , 73905-007-33 2000 ml in 1 bottle , 73905-007-34 2500 ml in 1 bottle , 73905-007-35 3000 ml in 1 bottle , 73905-007-36 3800 ml in 1 bottle , 73905-007-37 4000 ml in 1 bottle , 73905-007-38 5000 ml in 1 bottle , 73905-007-39 10000 ml in 1 bottle , 73905-007-40 20000 ml in 1 bottle , 73905-007-41 25000 ml in 1 bottle , 73905-007-42 45000 ml in 1 bottle , 73905-007-43 50000 ml in 1 bottle , 73905-007-44 100000 ml in 1 bottle , 73905-007-45 200000 ml in 1 bottle , 73905-007-46 500000 ml in 1 bottle , 73905-007-47 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 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 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".