NDC 51393-7591 Joint Pain Pain Management
Aesculus Hippocastanum Whole And Ruta Graveolens Whole Solution/ Drops Topical

Product Information

What is NDC 51393-7591?

The NDC code 51393-7591 is assigned by the FDA to the product Joint Pain Pain Management which is a human over the counter drug product labeled by Forces Of Nature. The generic name of Joint Pain Pain Management is aesculus hippocastanum whole and ruta graveolens whole. The product's dosage form is solution/ drops and is administered via topical form. The product is distributed in 3 packages with assigned NDC codes 51393-7591-1 11 ml in 1 bottle, dispensing , 51393-7591-2 33 ml in 1 bottle, dispensing , 51393-7591-4 4 ml in 1 bottle, dispensing . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code51393-7591
Proprietary Name 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.
Joint Pain Pain Management
Non-Proprietary Name 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.
Aesculus Hippocastanum Whole And Ruta Graveolens Whole
Product Type 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.
Human Otc Drug
Dosage FormSolution/ Drops - A solution which is usually administered in a drop-wise fashion.
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.
Forces Of Nature
Labeler Code51393
Marketing Category 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 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 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 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".
NDC Code Structure

What are the uses for Joint Pain Pain Management?

Product Packages

NDC Code 51393-7591-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC Code 51393-7591-2

Package Description: 33 mL in 1 BOTTLE, DISPENSING

NDC Code 51393-7591-4

Package Description: 4 mL in 1 BOTTLE, DISPENSING

Product Details

What are Joint Pain Pain Management Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Joint Pain Pain Management Active Ingredients UNII Codes

  • RUTA GRAVEOLENS WHOLE (UNII: 181JI0338P) (Active Moiety)

Joint Pain Pain Management Inactive Ingredients UNII Codes

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.

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Joint Pain Pain Management Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Manufactured by:
Forces of Nature, Inc.
21787 8th St East #3A
Sonoma, CA 95476 USA

Otc - Purpose

Active Ingredients
Aesculus Hippocastanum

USDA Certified Organic

30C -
Relieves Arthritis
Ruta Graveolens 30C - For Painful Joints

Also Contains

Sesame Oil, Lavandin Oil, Black Spruce Oil, German Chamomile Oil, Ginger Oil, Pine Oil, Cypress Oil, Rosemary Oil


For the temporary relief of minor aches and pains of muscles and joints associated with arthritis.


Shake well before use. Apply to affected area by gently rolling into the skin up to 3 or 4 times daily. For children under 2 years of age, consult a doctor before use.


Some individuals may be sensitive to essential oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin. For external use only. If accidental ingestion of more than several drops, and adverse reaction occurs, get medical help or contact a Poison Control Center. Do not apply to the eyes. If you are pregnant or breast-feeding, ask a health professional before use. Not for use on children under the age of 2 without physician direction.

Otc - Keep Out Of Reach Of Children

Keep all medicines out of the reach of children. Stop use and consult a doctor if condition worsens, or consult a doctor if symptoms show no improvement after 7 days.

Tips For Use

Application of Joint Pain Pain Management helps relieve pain by helping the system to reduce inflammation. Additionally, the lipophilic properties of the medicine help it penetrate deep into the tissue, relieving the pain. The relief is usually felt within just a few minutes of the application.

Joint Pain Pain Management should be applied at least 2-3 times per day every day or when you experience pain. For more severe and chronic pain the medicine may be used as needed for additional relief.

Simply apply the medicine directly to the site of pain or to your fingertip and gently rub it into the skin.

Principal Display Panel - 11 Ml Bottle Label


Joint Pain



.37 OZ/11 ml

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