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  4. NDC Product Code: 54039-001 Hand Sanitizer Gel(ag)

NDC 54039-001 Hand Sanitizer Gel(ag)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54039-001?
  5. Hand Sanitizer Gel(ag) 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:
54039-001
Proprietary Name:
Hand Sanitizer Gel(ag)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anhui Wanxing Industry Co.,ltd.
Labeler Code:
54039
Product Label ID:
a558e6b1-c33b-d002-e053-2a95a90a690f
Start Marketing Date: [9]
05-11-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Imprint(s):
SILVERELF

Product Packages

NDC Code 54039-001-01

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 54039-001?

The NDC code 54039-001 is assigned by the FDA to the product Hand Sanitizer Gel(ag) which is product labeled by Anhui Wanxing Industry Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54039-001-01 500 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(ag)?

Jput Proper Amount Of The Hand Sanitizer lnto Your Palm And Gently Rub it Over Your Palms,ths Back Of Your Hands,fingers And The Spaces Between your Fingers,rub Your Hands Together Continuously Until They Are Dry

Which are Hand Sanitizer Gel(ag) UNII Codes?

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

Which are Hand Sanitizer Gel(ag) 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".