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  4. NDC Product Code: 75940-127 Conazol

NDC 75940-127 Conazol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75940-127?
  4. Conazol Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75940-127
Proprietary Name:
Conazol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Marcasusa Llc
Labeler Code:
75940
Product Label ID:
54c2ead1-8b2d-4024-ab16-ae6bd2644994
Start Marketing Date: [9]
06-25-2014
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 75940-127?

The NDC code 75940-127 is assigned by the FDA to the product Conazol which is product labeled by Marcasusa Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75940-127-46 130 g 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 Conazol?

Wash affected area and dry thoroughlyshake can well and spray a thin layer over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot, pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyuse daily for 4 weeks for athlete's foot and ringworm; use daily for 2 weeks for jock itchif condition persists, consult a doctorthis product is not effective on the scalp or nailsin case of clogging, clear nozzle under running water

Which are Conazol UNII Codes?

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

Which are Conazol 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:

What is the NDC to RxNorm Crosswalk for Conazol?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".