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  4. NDC Product Code: 41254-009 Isopropyl Rubbing Alcohol 70%

NDC 41254-009 Isopropyl Rubbing Alcohol 70%

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41254-009?
  4. Isopropyl Rubbing Alcohol 70% 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:
41254-009
Proprietary Name:
Isopropyl Rubbing Alcohol 70%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Hawer Amenities Technology Co.,ltd
Labeler Code:
41254
Product Label ID:
a7c9121a-8e3a-5def-e053-2a95a90adeb7
Start Marketing Date: [9]
06-11-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41254-009-01

Package Description: 1000 mL in 1 BOTTLE

Product Details

What is NDC 41254-009?

The NDC code 41254-009 is assigned by the FDA to the product Isopropyl Rubbing Alcohol 70% which is product labeled by Jiangsu Hawer Amenities Technology Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41254-009-01 1000 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 Isopropyl Rubbing Alcohol 70%?

Take a small amount of product on the surface of the object until dry

Which are Isopropyl Rubbing Alcohol 70% UNII Codes?

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

Which are Isopropyl Rubbing Alcohol 70% 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".