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  4. NDC Product Code: 80105-1000 Straton

NDC 80105-1000 Straton

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80105-1000?
  4. Straton 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:
80105-1000
Proprietary Name:
Straton
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aerosoles Francomexicanos, S.a. De C.v.
Labeler Code:
80105
Product Label ID:
ae4d5ae2-3cb6-7a8e-e053-2a95a90a98d0
Start Marketing Date: [9]
09-01-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80105-1000-2

Package Description: 420 mL in 1 CAN

Product Details

What is NDC 80105-1000?

The NDC code 80105-1000 is assigned by the FDA to the product Straton which is product labeled by Aerosoles Francomexicanos, S.a. De C.v.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80105-1000-2 420 ml in 1 can . 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 Straton?

HANDS; SHAKE WELL BEFORE USING.HOLD CAN VERTICALLY 6 - 8 INCHES FROM THE PALM OF YOUR HANDS AND SPRAY ENOUGH ON THE PALM.RUB THE PALM OF YOUR HANDS AND FINGERTIPS UNTIL PRODUCT IS COMPLETELY DRY.

Which are Straton UNII Codes?

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

  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
  • N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)
  • N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) (UNII: 85440928RV) (Active Moiety)

Which are Straton 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".