1. Home
  2. Labeler Index
  3. Shantou Bomei Cosmetics Co., Ltd.
  4. NDC Product Code: 42085-002 Hand Sanitizer Gel

NDC 42085-002 Hand Sanitizer Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 42085-002?
  5. Hand Sanitizer Gel Uses
  6. Active Ingredients UNII Codes
  7. 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:
42085-002
Proprietary Name:
Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shantou Bomei Cosmetics Co., Ltd.
Labeler Code:
42085
Product Label ID:
a408181a-31c1-0ace-e053-2995a90afdcd
Start Marketing Date: [9]
04-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
RECTANGLE (C48347)

Product Packages

NDC Code 42085-002-01

Package Description: 100 mL in 1 BOTTLE

Product Details

What is NDC 42085-002?

The NDC code 42085-002 is assigned by the FDA to the product Hand Sanitizer Gel which is product labeled by Shantou Bomei Cosmetics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42085-002-01 100 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 Gel?

Take an appropriate amount of this product on the palm of your hand, rub your hands evenly to smear each part without rinsing.

Which are Hand Sanitizer Gel UNII Codes?

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

Which are Hand Sanitizer Gel 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:

* 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".