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  4. NDC Product Code: 54800-001 Disposable Hand Fluid

NDC 54800-001 Disposable Hand Fluid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54800-001?
  5. Disposable Hand Fluid 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:
54800-001
Proprietary Name:
Disposable Hand Fluid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Longgang Chengbao Industry Co., Ltd.
Labeler Code:
54800
Product Label ID:
a23d7002-dadf-2dbf-e053-2995a90a4f2c
Start Marketing Date: [9]
04-07-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)

Product Packages

NDC Code 54800-001-01

Package Description: 60 mL in 1 BOTTLE

Product Details

What is NDC 54800-001?

The NDC code 54800-001 is assigned by the FDA to the product Disposable Hand Fluid which is product labeled by Longgang Chengbao Industry Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54800-001-01 60 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 Disposable Hand Fluid?

External use disinfectant, not oral,

Which are Disposable Hand Fluid UNII Codes?

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

Which are Disposable Hand Fluid 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".