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  4. NDC Product Code: 75742-002 Green Island

NDC 75742-002 Green Island

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75742-002?
  4. Green Island Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75742-002
Proprietary Name:
Green Island
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Labeler Code:
75742
Product Label ID:
a7443a72-6ee5-07f7-e053-2995a90a3341
Start Marketing Date: [9]
06-04-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75742-002-01

Package Description: 30 mL in 1 BOTTLE

NDC Code 75742-002-02

Package Description: 53 mL in 1 BOTTLE

NDC Code 75742-002-03

Package Description: 59 mL in 1 BOTTLE

NDC Code 75742-002-04

Package Description: 60 mL in 1 BOTTLE

NDC Code 75742-002-05

Package Description: 80 mL in 1 BOTTLE

NDC Code 75742-002-06

Package Description: 100 mL in 1 BOTTLE

NDC Code 75742-002-07

Package Description: 120 mL in 1 BOTTLE

NDC Code 75742-002-08

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC Code 75742-002-09

Package Description: 375 mL in 1 BOTTLE, PUMP

NDC Code 75742-002-10

Package Description: 500 mL in 1 BOTTLE, PUMP

NDC Code 75742-002-11

Package Description: 1000 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 75742-002?

The NDC code 75742-002 is assigned by the FDA to the product Green Island which is product labeled by Zhejiang Guoyao Jingyue Aerosol Co., Ltd.. The product's dosage form is . The product is distributed in 11 packages with assigned NDC codes 75742-002-01 30 ml in 1 bottle , 75742-002-02 53 ml in 1 bottle , 75742-002-03 59 ml in 1 bottle , 75742-002-04 60 ml in 1 bottle , 75742-002-05 80 ml in 1 bottle , 75742-002-06 100 ml in 1 bottle , 75742-002-07 120 ml in 1 bottle , 75742-002-08 237 ml in 1 bottle, pump , 75742-002-09 375 ml in 1 bottle, pump , 75742-002-10 500 ml in 1 bottle, pump , 75742-002-11 1000 ml in 1 bottle, pump . 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 Green Island?

Apply on the surface of hands or other objects to be disinfected, stay 3 minutes until dry naturally.

Which are Green Island UNII Codes?

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

Which are Green Island 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:

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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".