FDA Registration No. 18101635346

FDA Unique Facility Identifier (UFI) No. 117356933

About Us

Risingsun Iodine Products Corp is a domestic corporation doing business in Montana since 1998. Risingsun manufactures all of its iodine supplements in a GMP Certified and FDA inspected facility located in the great state of Montana. 

 

Risingsun Iodine's History

Established in 1998

Risingsun has been manufacturing iodine supplements since 1998. The owner started Risinsun when his monther was diagmosed with cancer. A couple years later his older broth was too diagnosed cancer. Over the years he formulated more that 200 products. Over the years the FDA issued warning letters addressing label and health claims. The issues addressed in the warning letters were revised and then submitted to the FDA. The policy at the time addressing warning leters by the FDA was resonses submitted to the FDA were not replied to. So when the FDA addressed a label issue, a warning letter would be sent. Then in 2010, the FDA and Risingsun enterend in to a perminent consent decree. 
 

Entered Consent Decree 2010

Risingsun and the FDa entered into a perminant consent decree on November 4, 2010 at 2:30Pm. 

FDA Approved submitted Labels 2017

Risingsun has been manufacturing supplements since 1998 and have implemented some of the most stringent GMP practices. You as buyer of Risingsun supplements will be able to view COA's (Certificate of Analysis) for each product you purchase. Risingsun hopes that other supplement manufactures follow this policy and provide COA's for their products.

GMP Certification 2018

Risingsun has been manufacturing supplements since 1998 and have implemented some of the most stringent GMP practices. You as buyer of Risingsun supplements will be able to view COA's (Certificate of Analysis) for each product you purchase. Risingsun hopes that other supplement manufactures follow this policy and provide COA's for their products

SOP Manual Final Draft Submitted to FDA 2020

Risingsun sent the final draft of its SOP (Standard Operating Procedure) manual in August 2020. In 2018 Risingsun submited to the FDA its SOP manual which consisted of 60 pages. The FDA sent respose corespondence requesting revisions to the manual, as a result, the SOP manul went from 60 pages to over 275 pages. The FDA critiqued the SOP manual and Risingsun addressed recommendations. The latest SOP manual submitted to the FDA for review is now over 300 pages. Risingsun is the only supplement manufacture that the FDA has reviewed and made recommendation to a SOP manual.

FDA Approval to Resume Operations 2020

Risingsun has been manufacturing supplements since 1998 and have implemented some of the most stringent GMP practices. You as buyer of Risingsun supplements will be able to view COA's (Certificate of Analysis) for each product you purchase. Risingsun hopes that other supplement manufactures follow this policy and provide COA's for their products​​

 

Our Goal

Our goal and Risingsun Iodine Products is simple: provide the highest quality and purest iodine supplements available. To ensure we achieve this goal, our iodine products contain three ingredients; Potassium iodide, Iodine and distilled water. Risingsun uses potassium iodide from South America to make pure iodine crystals for our Lugol's iodine solutions. Since these crystals are made in house, we can assure our customers they are 100% free of toxins, heavy metals and allergens.
 
 

Why Risingsun Iodine Is Different

Risingsun Iodine Supplements:
  • Labels reviewed by FDA
  • ​GMP Certified facility
  • FDA inspected facility
  • Registered with state of Montana
  • Lowest detected heavy metal content of any iodine supplement on the market
  • Separate production areas for each product
Risingsun is the only iodine supplement manufacturer that has separate production areas for each product. This eliminates the possibility of cross contamination and ensures the purity, safety and sanitation of our supplements. 
 

Compare Iodine Products

Risingsun Iodine Products GMP Records

GMP Certification From Montana Manufacturing Extension Center 2310 University Way Building 2 Suite 1, Bozeman, MT 59717.
  1. FDA onsite inspection November 20, 2019
  2. DEA Registration to manufacture Lugol's Iodine over 2.2%
  3. Potassium Iodide COA
  4. Lugol's 2.2% Iodine Solution COA
  5. Lugol's 5% Iodine Solution COA