NDC 72053-001 Arthrocare Maximum Arthritis Pain Relief

Methyl Salicylate, Lidocaine

NDC Product Code 72053-001

NDC CODE: 72053-001

Proprietary Name: Arthrocare Maximum Arthritis Pain 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.

Non-Proprietary Name: Methyl Salicylate, Lidocaine 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.

NDC Code Structure

  • 72053 - Patient Focused Telehealth, Llc
    • 72053-001 - Arthrocare Maximum Arthritis Pain Relief

NDC 72053-001-01

Package Description: 1 TUBE in 1 BOX > 15 mL in 1 TUBE

NDC Product Information

Arthrocare Maximum Arthritis Pain Relief with NDC 72053-001 is a a human over the counter drug product labeled by Patient Focused Telehealth, Llc. The generic name of Arthrocare Maximum Arthritis Pain Relief is methyl salicylate, lidocaine. The product's dosage form is cream and is administered via topical form.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Arthrocare Maximum Arthritis Pain Relief 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.

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.

Product Labeler Information

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

Labeler Name: Patient Focused Telehealth, Llc
Labeler Code: 72053
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: 10-19-2021 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: 12-31-2022 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 - NO 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.

Arthrocare Maximum Arthritis Pain Relief Product Label Images

Arthrocare Maximum Arthritis Pain 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

Active Ingredients

Methyl Salicylate 15%Lidocaine 4%


Topical Analgesic


  • For temporary relief of minor aches and pains of muscles and joints associated with: arthritissimple backachemuscle strainssprainsbruisesjoint pain


For external use onlyUse only as directed. Read and follow all directions and warnings on this carton.Avoid contact with eyes and mucous membranes.

Do Not Use

  • At the same time as other topical analgesicson open wounds, cuts, damaged or infected skinwith bandage or heating pad

Consult Doctor Before Use

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Stop Use And Ask A Doctor If

  • Condition worsenssymptoms persist for more than 7 days or clear up and occur again within a few daysIf pregnant or breast-feeding or if you have sensitive skin, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

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


  • Apply 3 to 6 drops of product directly to affected areaProduct may be used as necessary, but should not be used more than four times per dayGently massage the product for 15 - 30 seconds into the skin over the site of pain (joint or muscle)

Inactive Ingredients

Ascorbic acid, aloe barbadensis leaf juice, carbomer, cholecalciferol, citric acid, diazolidinyl urea, dimethyl sulfoxide, dipropylene glycol, DMDM hydantoin, glycerin, polysorbate 20, sodium dodecylbenzene sulfonate, tetrasodium EDTA, tocopheryl acetate (vitamin E acetate), triethanolamine, water

* Please review the disclaimer below.