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  4. NDC Product Code: 71521-391 Diabetic Antifungal

NDC 71521-391 Diabetic Antifungal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71521-391?
  4. Diabetic Antifungal 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:
71521-391
Proprietary Name:
Diabetic Antifungal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lavior Inc
Labeler Code:
71521
Product Label ID:
bdbcf0c0-2cf3-6bd7-e053-2995a90ac3dd
Start Marketing Date: [9]
03-17-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71521-391-50

Package Description: 50 g in 1 BOTTLE, PUMP

Product Details

What is NDC 71521-391?

The NDC code 71521-391 is assigned by the FDA to the product Diabetic Antifungal which is product labeled by Lavior Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71521-391-50 50 g in 1 bottle, pump . 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 Diabetic Antifungal?

Read all warnings and directionsuse only as directedwash the affected area and dry thoroughlyapply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctorSupervise children in the use of this productfor athletes’ foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.this product is not effective on the scalp or nailswash hands after each use

Which are Diabetic Antifungal UNII Codes?

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

Which are Diabetic Antifungal 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".