Radiation Plus Liquid
NDC Package 43742-0945-1
Package Information
Radiation Plus (chondrus crispus, fucus vesiculosus, thyroidinum (suis), cadmium iodatum, cadmium sulphuratum, iodium, radium bromatum, strontium carbonicum, uranium nitricum, x-ray, arnica montana) liquids is for temporary relief from symptoms associated with radiation exposure, including weakness, fatigue, dehydration, and diarrhea.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-0945.
Identification & Billing
Clinical Specifications
- ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_X]/mL
- ARNICA MONTANA 30 [hp_C]/mL
- CADMIUM IODIDE 12 [hp_X]/mL
- CADMIUM SULFIDE 12 [hp_X]/mL
- CHONDRUS CRISPUS 3 [hp_X]/mL
- FUCUS VESICULOSUS 3 [hp_X]/mL
- IODINE 12 [hp_X]/mL
- RADIUM BROMIDE 12 [hp_X]/mL
- STRONTIUM CARBONATE 12 [hp_X]/mL
- SUS SCROFA THYROID 8 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-0945 - Radiation Plus
- 43742-0945-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-0945 - Radiation Plus
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43742-0945-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Radiation Plus, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains alcohol, x-ray exposed (1000 rad); arnica montana; cadmium iodide; cadmium sulfide; chondrus crispus; fucus vesiculosus; iodine; radium bromide; strontium carbonate; sus scrofa thyroid; uranyl nitrate hexahydrate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Deseret Biologicals, Inc. on December 28, 2016.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742094501. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.