NDC 73563-080 Antibacterial 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:
73563-080
Proprietary Name:
Antibacterial Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Body One Products , Inc.
Labeler Code:
73563
Start Marketing Date: [9]
03-10-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 73563-080-01

Package Description: 29.5 mL in 1 TUBE

NDC Code 73563-080-02

Package Description: 59 mL in 1 BOTTLE

NDC Code 73563-080-04

Package Description: 3785 mL in 1 BOTTLE

NDC Code 73563-080-06

Package Description: 66 mL in 1 TUBE

NDC Code 73563-080-07

Package Description: 7 mL in 1 PACKET

NDC Code 73563-080-08

Package Description: 236 mL in 1 BOTTLE

NDC Code 73563-080-12

Package Description: 355 mL in 1 BOTTLE, PUMP

NDC Code 73563-080-18

Package Description: 532 mL in 1 BOTTLE

Product Details

What is NDC 73563-080?

The NDC code 73563-080 is assigned by the FDA to the product Antibacterial Hand Sanitizer which is product labeled by Body One Products , Inc.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 73563-080-01 29.5 ml in 1 tube , 73563-080-02 59 ml in 1 bottle , 73563-080-04 3785 ml in 1 bottle , 73563-080-06 66 ml in 1 tube , 73563-080-07 7 ml in 1 packet , 73563-080-08 236 ml in 1 bottle , 73563-080-12 355 ml in 1 bottle, pump , 73563-080-18 532 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 Antibacterial Hand Sanitizer?

Wet hands thoroughly with productbriskly rub hands together until drysupervise children in the use of this product

Which are Antibacterial Hand Sanitizer UNII Codes?

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

Which are Antibacterial 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 Antibacterial 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".