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NDC 85398-018 Hermon Athletes Foot Tolnaftate 1% Kit

Tolnaftate 1% Kit Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 85398-018?
  4. Hermon Athletes Foot Tolnaftate 1% Kit Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

Get all the details for National Drug Code (NDC) 85398-018 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
85398-018
Proprietary Name:
Hermon Athletes Foot Tolnaftate 1% Kit
Non-Proprietary Name: [1]
Tolnaftate 1% Kit
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s): [4]
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler Name: [5]
Beautivity Llc
Labeler Code:
85398
Product Label ID:
4142f490-c4b5-a9f3-e063-6394a90ab75e
FDA Application Number: [6]
M005
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
10-31-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 85398-018?

The NDC code 85398-018 is assigned by the FDA to the product Hermon Athletes Foot Tolnaftate 1% Kit which is a human over the counter drug product labeled by Beautivity Llc. The generic name of Hermon Athletes Foot Tolnaftate 1% Kit is tolnaftate 1% kit. The product's dosage form is kit and is administered via topical form. The product is distributed in a single package with assigned NDC code 85398-018-01 1 kit in 1 carton * 57 g in 1 tube (85398-017-02) * 116 g in 1 carton (85398-007-02). 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 Hermon Athletes Foot Tolnaftate 1% Kit?

Directions (Cream)adults and children 12 years and overuse the tip of thecap to break the seal and open the tubewash the affedted skin with soap and water and dry completely before applyingfor athlete's foot wear well-fitting, ventilated shoes. Change shoes and socks at least once daily.between the ttoes only: apply twice a day (morning and night) for 1 week or as directed by a doctoron the bottom or sides ofthe foot: apply twice a day (morning and night) for 2 weeks or as directed by a doctorfor jock itch and ringworm: apply oncea day (morning or night) for 1 week or as directed by a doctorwash hands after each usechildren under 12 years: ask a doctorwash affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night)supervise children in the use of this productuse daily for2 weeks Directions (Soap Bar) Wet skin with warm water and lather soap.Gently massage onto affeected areas.Rinse thoroughly and dry.Use twice daily or as directed by a doctor.

Which are Hermon Athletes Foot Tolnaftate 1% Kit UNII Codes?

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

Which are Hermon Athletes Foot Tolnaftate 1% Kit 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 Hermon Athletes Foot Tolnaftate 1% Kit?

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

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

[6] 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.

[8] 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.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".