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  4. NDC Product Code: 78422-001 Mu Instant Hand Sanitizer

NDC 78422-001 Mu Instant Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78422-001?
  4. Mu Instant 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:
78422-001
Proprietary Name:
Mu Instant Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ningbo Royal Union Co., Ltd.
Labeler Code:
78422
Product Label ID:
73283c83-2cdf-48cb-a08c-328bfeae1b89
Start Marketing Date: [9]
05-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78422-001-01

Package Description: 10 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-02

Package Description: 20 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-03

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-04

Package Description: 45 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-05

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-06

Package Description: 55 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-07

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-08

Package Description: 80 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-09

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-10

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-11

Package Description: 180 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-12

Package Description: 200 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-13

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-14

Package Description: 250 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-15

Package Description: 300 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-16

Package Description: 474 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-17

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-18

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-19

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-20

Package Description: 2000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-21

Package Description: 3000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-22

Package Description: 4000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-23

Package Description: 5000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-24

Package Description: 10000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-25

Package Description: 20000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-26

Package Description: 50000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-27

Package Description: 100000 mL in 1 BOTTLE, PLASTIC

NDC Code 78422-001-28

Package Description: 980 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 78422-001?

The NDC code 78422-001 is assigned by the FDA to the product Mu Instant Hand Sanitizer which is product labeled by Ningbo Royal Union Co., Ltd.. The product's dosage form is . The product is distributed in 28 packages with assigned NDC codes 78422-001-01 10 ml in 1 bottle, plastic , 78422-001-02 20 ml in 1 bottle, plastic , 78422-001-03 30 ml in 1 bottle, plastic , 78422-001-04 45 ml in 1 bottle, plastic , 78422-001-05 50 ml in 1 bottle, plastic , 78422-001-06 55 ml in 1 bottle, plastic , 78422-001-07 60 ml in 1 bottle, plastic , 78422-001-08 80 ml in 1 bottle, plastic , 78422-001-09 100 ml in 1 bottle, plastic , 78422-001-10 120 ml in 1 bottle, plastic , 78422-001-11 180 ml in 1 bottle, plastic , 78422-001-12 200 ml in 1 bottle, plastic , 78422-001-13 237 ml in 1 bottle, plastic , 78422-001-14 250 ml in 1 bottle, plastic , 78422-001-15 300 ml in 1 bottle, plastic , 78422-001-16 474 ml in 1 bottle, plastic , 78422-001-17 500 ml in 1 bottle, plastic , 78422-001-18 946 ml in 1 bottle, plastic , 78422-001-19 1000 ml in 1 bottle, plastic , 78422-001-20 2000 ml in 1 bottle, plastic , 78422-001-21 3000 ml in 1 bottle, plastic , 78422-001-22 4000 ml in 1 bottle, plastic , 78422-001-23 5000 ml in 1 bottle, plastic , 78422-001-24 10000 ml in 1 bottle, plastic , 78422-001-25 20000 ml in 1 bottle, plastic , 78422-001-26 50000 ml in 1 bottle, plastic , 78422-001-27 100000 ml in 1 bottle, plastic , 78422-001-28 980 ml in 1 bottle, plastic . 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 Mu Instant 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 Mu Instant Hand Sanitizer UNII Codes?

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

Which are Mu Instant 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 Mu Instant 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".