NDC 72342-190 Pain Relief Roll-on Muscle

Camphor (natural)

NDC Product Code 72342-190

NDC 72342-190-85

Package Description: 85 g in 1 BOTTLE, WITH APPLICATOR

NDC Product Information

Pain Relief Roll-on Muscle with NDC 72342-190 is a a human over the counter drug product labeled by J.r. Watkins, Llc.. The generic name of Pain Relief Roll-on Muscle is camphor (natural). The product's dosage form is gel and is administered via topical form.

Labeler Name: J.r. Watkins, Llc.

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 Roll-on Muscle 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.

  • CAMPHOR (NATURAL) 1.5 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • 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: J.r. Watkins, Llc.
Labeler Code: 72342
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: 12-15-2020 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: 12-31-2021 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 Roll-on Muscle Product Label Images

Pain Relief Roll-on Muscle 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

Active Ingredient

Camphor 1.5%


Topical Analgesic


For the temporary relief of pain


For external use only.Flammable: Keep away from fire or flame and heated surfaces.

Do Not Use

  • On open wounds, damaged or irritated skinWith a heading pad or TENS deviceWith any other creams, ointments, sprays, liniments, or other topical products containing camphor

When Using This Product

  • Do not bandage tightlyUse only as directedAvoid contact with eyes or mucous membranes

Stop Use And Ask A Doctor If

  • Condition worsensRash, itching, redness, or excessive irritation of skin developsSymptoms persist for more than 7 daysSymptoms clear up and occur again within a few days

If Pregnant Or Breastfeeding

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 a Poison Control Center right away.


  • Adults and children 12 years of age and older: Apply to affected area not more 4 times a dayMassage painful area until absorbed into skinWash hands after each use with cold waterChildren under 12 years of age: consult a doctor.

Other Information

  • Store away from childrenStore in dry, well-ventilated conditions at room temperature (59-77°F)

Inactive Ingredients

Arnica montana flower extract, cholecalciferol, denatured alcohol, ethylhexylglycerin, glycerin, hydroxyethylcellulose, magnesium chloride hexahydrate, Mentha piperita (peppermint) oil, phenoxyethanol, polysorbate 20, water

* Please review the disclaimer below.