NDC 29784-141 Quinsana Athletes Foot Anti Fungal

Tolnaftate

NDC Product Code 29784-141

NDC 29784-141-85

Package Description: 85 g in 1 BOTTLE

NDC Product Information

Quinsana Athletes Foot Anti Fungal with NDC 29784-141 is a a human over the counter drug product labeled by Profoot, Inc.. The generic name of Quinsana Athletes Foot Anti Fungal is tolnaftate. The product's dosage form is powder and is administered via topical form.

Labeler Name: Profoot, Inc.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Quinsana Athletes Foot Anti Fungal Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TOLNAFTATE 10 mg/g

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.

  • TALC (UNII: 7SEV7J4R1U)
  • STARCH, CORN (UNII: O8232NY3SJ)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Profoot, Inc.
Labeler Code: 29784
FDA Application Number: part333C What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-01-2019 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: 12-31-2020 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Quinsana Athletes Foot Anti Fungal Product Label Images

Quinsana Athletes Foot Anti Fungal 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

Active Ingredient

Tolnaftate, 1%

Purpose

Antifungal

Uses

  • Cures most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis)Effectively relieves itching, cracking, and burning

Warnings

For external use only

Ask A Doctor Before Use

  • On children under 2 years of age

When Using This Product

  • Avoid contact with eyes

Stop Use And Ask A Doctor If

  • Irritation occursthere is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)

Keep Out Of Reach Of Children.

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

Directions

  • Wash affected area and dry thoroughly.Apply a thin layer of the product over time indicated.Supervise children in the use of this product.
  • For athlete's foot and ringworm: Use twice daily (morning and night) for 4 weeks or as directed by physician. Pay special attention to spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
  • For jock itch: Use daily for 2 weeks.
  • Clean the affected area and dry thoroughly.This product is not effective on the scalp or nails.

Inactive Ingredients

Talc, Cornstarch.

* Please review the disclaimer below.

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