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  4. NDC Product Code: 43251-3353 Flexitol First Aid

NDC 43251-3353 Flexitol First Aid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43251-3353?
  4. Flexitol First Aid Uses
  5. Active 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:
43251-3353
Proprietary Name:
Flexitol First Aid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laderma Trading Pty Ltd
Labeler Code:
43251
Product Label ID:
9d366317-c1e5-41e8-bc8f-f165a4fa06f0
Start Marketing Date: [9]
03-12-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43251-3353-7

Package Description: 1 TUBE in 1 CARTON / 60 mL in 1 TUBE

Product Details

What is NDC 43251-3353?

The NDC code 43251-3353 is assigned by the FDA to the product Flexitol First Aid which is product labeled by Laderma Trading Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43251-3353-7 1 tube in 1 carton / 60 ml in 1 tube. 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 Flexitol First Aid?

Rinse wound with warm water Spray onto affected area and absorb excess liquid with a cotton ballUse as required or as directed by a physicianFor best results use in conjunction with Natralia First Aid Cream

Which are Flexitol First Aid UNII Codes?

The UNII codes for the active 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".