NDC 51393-4015 Back Pain Pain Management

Arnica Montana, Horse Chestnut, Hypericum Perforatum, Ruta Graveolens Whole, And Sodium Chloride

NDC Product Code 51393-4015

NDC CODE: 51393-4015

Proprietary Name: Back Pain Pain Management 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: Arnica Montana, Horse Chestnut, Hypericum Perforatum, Ruta Graveolens Whole, And Sodium Chloride 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

NDC 51393-4015-1

Package Description: 1 BOTTLE, DISPENSING in 1 CARTON > 11 mL in 1 BOTTLE, DISPENSING

NDC 51393-4015-4

Package Description: 1 BOTTLE, DISPENSING in 1 CARTON > 4 mL in 1 BOTTLE, DISPENSING

NDC Product Information

Back Pain Pain Management with NDC 51393-4015 is a a human over the counter drug product labeled by Forces Of Nature. The generic name of Back Pain Pain Management is arnica montana, horse chestnut, hypericum perforatum, ruta graveolens whole, and sodium chloride. The product's dosage form is solution/ drops and is administered via topical form.

Labeler Name: Forces Of Nature

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

Back Pain Pain Management 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.

  • ARNICA MONTANA 30 [hp_C]/100mL
  • HORSE CHESTNUT 6 [hp_C]/100mL
  • SODIUM CHLORIDE 30 [hp_C]/100mL

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: Forces Of Nature
Labeler Code: 51393
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 11-01-2019 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’.

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Back Pain Pain Management Product Label Images