NDC 65734-348 Fungus Relief

NDC Product Code 65734-348

NDC CODE: 65734-348

Proprietary Name: Fungus Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 65734 - Swabplus Inc.

NDC 65734-348-36

Package Description: 36 APPLICATOR in 1 PACKAGE > .15 mL in 1 APPLICATOR (65734-348-00)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Fungus Relief with NDC 65734-348 is a product labeled by Swabplus Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 313423.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Swabplus Inc.
Labeler Code: 65734
Start Marketing Date: 03-01-2003 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Information for Patients

Tolnaftate

Tolnaftate is pronounced as (tole naf' tate)

Why is tolnaftate medication prescribed?
Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm.This medication is sometimes prescribed for other uses;...
[Read More]

* Please review the disclaimer below.

Fungus Relief Product Label Images

Fungus Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts

Active Ingredient Tolnaftate 1%

Purpose

Antifungal

Uses

  • Cures fungal infections of the toes and fingers, including skin around and under nails, where accessible with swab applicator. Cures most athlete's foot (tinea pedis) and ringworm (tinea corporis) and relieves symptoms of athlete's foot including itching, burning and scaly skin. Help prevent most athlete's foot from recuring when uses daily.

Warings

For external use only.When using this product avoid contact with eyes.Stop use and ask a doctor if irritation occurs. there is no improvement within 4 weeks.Do not use on children under 2 years of age except under the advice and supervision of a doctor.

Keep Out Of The Reach Of Children

If swallowed get  medical help or contact a Poison Control Center right away.

Directions

  • 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.

Other Information

Avoid storing at excessive heat.

Inactive Ingredients

Aloe Barbadensis Leaf Extract. BHT. Butylene Glycol, Diazolidinyl Urea, Ethoxydiglycol, Methylparaben, Propylene Glycol, Propylparaben. Tocopheryl Acetate

* Please review the disclaimer below.