NDC 71341-001 Athletesgel

Capsaicin, Menthol, Methyl Salicylate

NDC Product Code 71341-001

NDC 71341-001-20

Package Description: 1 TUBE in 1 CARTON > 20 g in 1 TUBE

NDC 71341-001-50

Package Description: 1 TUBE in 1 CARTON > 50 g in 1 TUBE

NDC 71341-001-80

Package Description: 1 TUBE in 1 CARTON > 80 g in 1 TUBE

NDC Product Information

Athletesgel with NDC 71341-001 is a a human over the counter drug product labeled by Hammock Pharmaceuticals, Inc.. The generic name of Athletesgel is capsaicin, menthol, methyl salicylate. The product's dosage form is gel and is administered via topical form.

Labeler Name: Hammock Pharmaceuticals, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Athletesgel 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.

  • CAPSAICIN .025 g/100g

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.

  • CLOVE OIL (UNII: 578389D6D0)
  • ALLANTOIN (UNII: 344S277G0Z)

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.
  • 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: Hammock Pharmaceuticals, Inc.
Labeler Code: 71341
FDA Application Number: part348 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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 10-01-2019 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.

Athletesgel Product Label Images

Athletesgel 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

Distributed by:Hammock Pharmaceuticals.Charlotte, NC 28723 USAwww.athletesgel.usLicensed by Athletes Gel. Manufactured in Australia.

Otc - Active Ingredient

Active ingredientsCapsaicin 0.025%Menthol 8%Methyl salicylate 27%

Otc - Purpose

PurposeTopical analgesicTopical analgesicTopical analgesic

Indications & Usage

  • Uses Temporarily relieves the minor aches, pains and inflammation of muscles and joints associated with:
  • Strainssprainsbruisesarthritis


WarningsFor external use only

Otc - Do Not Use

  • Do not useon wounds or damaged skinwith a heating padon a child under 12 years of age with arthritis-like conditions

Otc - When Using

  • When using this productavoid contact with eyes and mucous membranesdo not bandage tightly

Otc - Stop Use

  • Stop use and ask a doctor ifcondition worsens or symptoms last more than 7 days or clear upcondition clears up and occurs again within a few daysexcessive rash or irritation develops

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

  • Directionsuse only as directedadults and children 12 years and over:apply to affected area not more than 3 times dailystart with a small amount to assess heat before applying morewash hands with soap and water after usechildren under 12 years of age: ask a doctor

Storage And Handling

Other information
store at 20° to 25°C (68° to 77°F)

Inactive Ingredient

Inactive ingredientsallantoin, almond oil, arnica, clove bud oil, colloidal anhydrous silica, diethylene glycol monoethyl ether

Otc - Questions

Questions? 877-323-6999

* Please review the disclaimer below.