1. Home
  2. Labeler Index
  3. Guangzhou Oumiao Cosmetics Co. Ltd.
  4. NDC Product Code: 74761-011 Antibacterial Hand Sanitizer

NDC 74761-011 Antibacterial Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74761-011?
  4. Antibacterial Hand Sanitizer Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
74761-011
Proprietary Name:
Antibacterial Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Oumiao Cosmetics Co. Ltd.
Labeler Code:
74761
Product Label ID:
a69fb66e-8dcf-31cd-e053-2995a90a2d9d
Start Marketing Date: [9]
04-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74761-011-01

Package Description: 30 mL in 1 BOTTLE

NDC Code 74761-011-02

Package Description: 50 mL in 1 BOTTLE

NDC Code 74761-011-03

Package Description: 60 mL in 1 BOTTLE

NDC Code 74761-011-04

Package Description: 100 mL in 1 BOTTLE

NDC Code 74761-011-05

Package Description: 200 mL in 1 BOTTLE

NDC Code 74761-011-06

Package Description: 250 mL in 1 BOTTLE

NDC Code 74761-011-07

Package Description: 300 mL in 1 BOTTLE

NDC Code 74761-011-08

Package Description: 500 mL in 1 BOTTLE

NDC Code 74761-011-09

Package Description: 1000 mL in 1 BOTTLE

NDC Code 74761-011-10

Package Description: 2000 mL in 1 BOTTLE

NDC Code 74761-011-11

Package Description: 1 mL in 1 BAG

NDC Code 74761-011-12

Package Description: 2 mL in 1 BAG

NDC Code 74761-011-13

Package Description: 3 mL in 1 BAG

NDC Code 74761-011-14

Package Description: 5 mL in 1 BAG

NDC Code 74761-011-15

Package Description: 6 mL in 1 BAG

NDC Code 74761-011-16

Package Description: 8 mL in 1 BAG

NDC Code 74761-011-17

Package Description: 10 mL in 1 BAG

NDC Code 74761-011-18

Package Description: 15 mL in 1 BAG

NDC Code 74761-011-19

Package Description: 20 mL in 1 BAG

NDC Code 74761-011-20

Package Description: 25 mL in 1 BAG

NDC Code 74761-011-21

Package Description: 35 mL in 1 BOTTLE

NDC Code 74761-011-22

Package Description: 45 mL in 1 BOTTLE

NDC Code 74761-011-23

Package Description: 75 mL in 1 BOTTLE

NDC Code 74761-011-24

Package Description: 80 mL in 1 BOTTLE

NDC Code 74761-011-25

Package Description: 120 mL in 1 BOTTLE

NDC Code 74761-011-26

Package Description: 260 mL in 1 BOTTLE

NDC Code 74761-011-27

Package Description: 600 mL in 1 BOTTLE

NDC Code 74761-011-28

Package Description: 750 mL in 1 BOTTLE

NDC Code 74761-011-29

Package Description: 800 mL in 1 BOTTLE

NDC Code 74761-011-30

Package Description: 3785 mL in 1 BOTTLE

NDC Code 74761-011-31

Package Description: 3000 mL in 1 BOTTLE

NDC Code 74761-011-32

Package Description: 4000 mL in 1 BOTTLE

NDC Code 74761-011-33

Package Description: 5000 mL in 1 BOTTLE

NDC Code 74761-011-34

Package Description: 6000 mL in 1 BOTTLE

NDC Code 74761-011-35

Package Description: 8000 mL in 1 BOTTLE

NDC Code 74761-011-36

Package Description: 10000 mL in 1 BOTTLE

NDC Code 74761-011-37

Package Description: 20000 mL in 1 BOTTLE

NDC Code 74761-011-38

Package Description: 30000 mL in 1 BOTTLE

NDC Code 74761-011-39

Package Description: 50000 mL in 1 BOTTLE

NDC Code 74761-011-40

Package Description: 75000 mL in 1 BOTTLE

NDC Code 74761-011-41

Package Description: 80000 mL in 1 BOTTLE

NDC Code 74761-011-42

Package Description: 100000 mL in 1 BOTTLE

NDC Code 74761-011-43

Package Description: 200000 mL in 1 BOTTLE

NDC Code 74761-011-44

Package Description: 300000 mL in 1 BOTTLE

NDC Code 74761-011-45

Package Description: 400000 mL in 1 BOTTLE

NDC Code 74761-011-46

Package Description: 500000 mL in 1 BOTTLE

NDC Code 74761-011-47

Package Description: 600000 mL in 1 BOTTLE

NDC Code 74761-011-48

Package Description: 750000 mL in 1 BOTTLE

NDC Code 74761-011-49

Package Description: 800000 mL in 1 BOTTLE

NDC Code 74761-011-50

Package Description: 1000000 mL in 1 BOTTLE

NDC Code 74761-011-51

Package Description: 1200000 mL in 1 BOTTLE

NDC Code 74761-011-52

Package Description: 2000000 mL in 1 BOTTLE

NDC Code 74761-011-53

Package Description: 5000000 mL in 1 BOTTLE

NDC Code 74761-011-54

Package Description: 10000000 mL in 1 BOTTLE

Product Details

What is NDC 74761-011?

The NDC code 74761-011 is assigned by the FDA to the product Antibacterial Hand Sanitizer which is product labeled by Guangzhou Oumiao Cosmetics Co. Ltd.. The product's dosage form is . The product is distributed in 54 packages with assigned NDC codes 74761-011-01 30 ml in 1 bottle , 74761-011-02 50 ml in 1 bottle , 74761-011-03 60 ml in 1 bottle , 74761-011-04 100 ml in 1 bottle , 74761-011-05 200 ml in 1 bottle , 74761-011-06 250 ml in 1 bottle , 74761-011-07 300 ml in 1 bottle , 74761-011-08 500 ml in 1 bottle , 74761-011-09 1000 ml in 1 bottle , 74761-011-10 2000 ml in 1 bottle , 74761-011-11 1 ml in 1 bag , 74761-011-12 2 ml in 1 bag , 74761-011-13 3 ml in 1 bag , 74761-011-14 5 ml in 1 bag , 74761-011-15 6 ml in 1 bag , 74761-011-16 8 ml in 1 bag , 74761-011-17 10 ml in 1 bag , 74761-011-18 15 ml in 1 bag , 74761-011-19 20 ml in 1 bag , 74761-011-20 25 ml in 1 bag , 74761-011-21 35 ml in 1 bottle , 74761-011-22 45 ml in 1 bottle , 74761-011-23 75 ml in 1 bottle , 74761-011-24 80 ml in 1 bottle , 74761-011-25 120 ml in 1 bottle , 74761-011-26 260 ml in 1 bottle , 74761-011-27 600 ml in 1 bottle , 74761-011-28 750 ml in 1 bottle , 74761-011-29 800 ml in 1 bottle , 74761-011-30 3785 ml in 1 bottle , 74761-011-31 3000 ml in 1 bottle , 74761-011-32 4000 ml in 1 bottle , 74761-011-33 5000 ml in 1 bottle , 74761-011-34 6000 ml in 1 bottle , 74761-011-35 8000 ml in 1 bottle , 74761-011-36 10000 ml in 1 bottle , 74761-011-37 20000 ml in 1 bottle , 74761-011-38 30000 ml in 1 bottle , 74761-011-39 50000 ml in 1 bottle , 74761-011-40 75000 ml in 1 bottle , 74761-011-41 80000 ml in 1 bottle , 74761-011-42 100000 ml in 1 bottle , 74761-011-43 200000 ml in 1 bottle , 74761-011-44 300000 ml in 1 bottle , 74761-011-45 400000 ml in 1 bottle , 74761-011-46 500000 ml in 1 bottle , 74761-011-47 600000 ml in 1 bottle , 74761-011-48 750000 ml in 1 bottle , 74761-011-49 800000 ml in 1 bottle , 74761-011-50 1000000 ml in 1 bottle , 74761-011-51 1200000 ml in 1 bottle , 74761-011-52 2000000 ml in 1 bottle , 74761-011-53 5000000 ml in 1 bottle , 74761-011-54 10000000 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?

Place enough Product.in your palm to thoroughly spread on both hands and rub into the skin until dry.Children under 6 years of age should be supervised when using 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:

* Please review the disclaimer below.

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".