NDC 73183-100 Dr. Phillips Formulations Muscle Joint Relief

Menthol, Methyl Salicylate, Camphor Bark Oil, Eucalyptus Leaf Oil

NDC Product Code 73183-100

NDC CODE: 73183-100

Proprietary Name: Dr. Phillips Formulations Muscle Joint 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: Menthol, Methyl Salicylate, Camphor Bark Oil, Eucalyptus Leaf Oil 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

  • 73183 - Dr. Phillips Formulations, Llc
    • 73183-100 - Dr. Phillips Formulations Muscle Joint Relief

NDC 73183-100-11

Package Description: 95500 mg in 1 BOTTLE, PUMP

NDC Product Information

Dr. Phillips Formulations Muscle Joint Relief with NDC 73183-100 is a a human over the counter drug product labeled by Dr. Phillips Formulations, Llc. The generic name of Dr. Phillips Formulations Muscle Joint Relief is menthol, methyl salicylate, camphor bark oil, eucalyptus leaf oil. The product's dosage form is cream and is administered via topical form.

Labeler Name: Dr. Phillips Formulations, Llc

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.

Dr. Phillips Formulations Muscle Joint 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.

  • MENTHOL 10 mg/100mg
  • METHYL SALICYLATE 10 mg/100mg
  • EUCALYPTUS OIL 2 mg/100mg
  • CAMPHOR (NATURAL) 3 mg/100mg

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: Dr. Phillips Formulations, Llc
Labeler Code: 73183
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: 07-29-2019 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.

Dr. Phillips Formulations Muscle Joint Relief Product Label Images

Dr. Phillips Formulations Muscle Joint 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

Otc - Active Ingredient

Menthol - 10%Methyl Salicylate - 10%Camphor Oil - 3%Eucalyptus Oil - 2%

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Purpose

For temporary relief of minor aches and pains of muscles and joints.

Dosage & Administration

Rub onto affected area 3 to 4 times daily. Clean area prior to application.


Keep out of reach of children. For external use only. Do not use on wounds or damaged skin, on mouth, avoid contact with eyes, genitals or any other mucous membrane, with a heating pad, or if condition worsens. If swallowed, get medical help or contact Poison Control Center.

Indications & Usage

For temporary relief of minor aches and pains of muscles and joints.

Inactive Ingredient

Aqua, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside, Cetearyl Alcohol, Cinnamomum Camphora, Glyceryl Stearate Citrate, CBD Hemp Extract, Prganic Aloe Barbadensis (Aloe Vera) leaf Juice, Tapioca Starch Modified, CLycerin, Caprylic, Capric Triglyceride, Xanthan Gum, Organic Rosmariun Officianalis (Rosemary) Leaf Extract, Organic Arnica Extract, Glyceryl Caprylate, Caprylhydroxamic Acid, Citric Acid

* Please review the disclaimer below.