NDC 51393-7522 Rheumatoid Arthritis Pain Management

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51393-7522
Proprietary Name:
Rheumatoid Arthritis Pain Management
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Forces Of Nature
Labeler Code:
51393
Start Marketing Date: [9]
01-01-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51393-7522-1

Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 11 mL in 1 BOTTLE, DISPENSING

NDC Code 51393-7522-2

Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 33 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 51393-7522?

The NDC code 51393-7522 is assigned by the FDA to the product Rheumatoid Arthritis Pain Management which is product labeled by Forces Of Nature. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51393-7522-1 1 bottle, dispensing in 1 box / 11 ml in 1 bottle, dispensing, 51393-7522-2 1 bottle, dispensing in 1 box / 33 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 and RxNorm crosswalk.

What are the uses for Rheumatoid Arthritis Pain Management?

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

Which are Rheumatoid Arthritis Pain Management UNII Codes?

The UNII codes for the active ingredients in this product are:

  • HORSE CHESTNUT (UNII: 3C18L6RJAZ)
  • HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
  • CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
  • CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)

Which are Rheumatoid Arthritis 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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".