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  4. NDC Product Code: 65734-348 Fungus Relief

NDC 65734-348 Fungus Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65734-348?
  4. Fungus Relief 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:
65734-348
Proprietary Name:
Fungus Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Swabplus Inc.
Labeler Code:
65734
Product Label ID:
3c60459f-19c3-479a-b17e-ac0cbd9dc75e
Start Marketing Date: [9]
03-01-2003
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 65734-348?

The NDC code 65734-348 is assigned by the FDA to the product Fungus Relief which is product labeled by Swabplus Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65734-348-36 36 applicator in 1 package / .15 ml in 1 applicator (65734-348-00). 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 Fungus Relief?

Do not use if label seal is broken prior to purchase.Keep swabs in original container when not in use.wash affected area and dry thoroughly.Hold the swab vertically with the color band tip upwards.Bend the tip at the color band to one side until it snaps.Apply a thin layer over affected area twice daily (morning and night)Discard swab after use.For athlete's foot, apply once or twice daily, pay special attention to spaces between toes, wear shoes with good ventilation and change shoes and socks at least once daily.Use daily for 4 weeks; if condition persists longer, ask a doctor.This product is not effective on the scalp or nails.

Which are Fungus Relief UNII Codes?

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

Which are Fungus Relief 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 Fungus Relief?

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".