NDC 73239-1904 Pain Relief Gel

Camphor, And Menthol Gel

NDC Product Code 73239-1904

NDC 73239-1904-1

Package Description: 100 mL in 1 TUBE

NDC Product Information

Pain Relief Gel with NDC 73239-1904 is a a human over the counter drug product labeled by Kanamed Inc.. The generic name of Pain Relief Gel is camphor, and menthol gel. The product's dosage form is gel and is administered via topical form.

Labeler Name: Kanamed 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.

Pain Relief Gel 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.

  • MENTHOL 5 mg/100mL
  • CAMPHOR (NATURAL) 5 mg/100mL

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.

  • WATER (UNII: 059QF0KO0R)

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: Kanamed Inc.
Labeler Code: 73239
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: 10-16-2019 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.

Pain Relief Gel Product Label Images

Pain Relief Gel 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

Otc - Active Ingredient

Menthol 5% Topical AnalgesicCamphor 5% Topical Analgesic

Indications & Usage

  • Temporarily relieves minor aches and pains of muscles and joints associated witharthritissimple backachemuscle strainsbruisessprains

Inactive Ingredient

  • Hemp seed oilAloe vera JuicePeppermint OilEthylenediaminetetraacetic AcidGlycerineCarbopol U10Caustic Soda/Sodium hydroxidePropylene GlycolSodium BenzonateDM Water

Dosage & Administration

Use only as directed

Adults and children 12 years of age and older apply to affected area not more than 3 to 4 times daily

Children under the age of 12 years of age consult a doctor


  • For external use onlyOnly use as directedDo not allow contact with eyesDo not bandage tightlySTOP use and ask a doctor if:symptoms last more than 7 days or clear up and occur again within a few daysExcessive skin irritation occurs If you have redness over the affected area

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Purpose

Topical Analgesic

Other Safety Information

Store at room temperature

* Please review the disclaimer below.