Gum Therapy Liquid
NDC Package 43742-1509-1
Package Information
Gum Therapy (calendula officinalis, kali phosphoricum, natrum muriaticum, arnica montana, agave americana, cistus canadensis, kreosotum, myrrha, calcarea fluorica, aconitum napellus, bismuthum subnitricum, sepia, hepar sulphuris calcareum, mercurius vivus) liquids is for temporary relief of symptoms related to gingivitis, inflamed and bleeding gums and minor pain.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, this product is identified by NDC 43742-1509.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 12 [hp_X]/mL
- AGAVE AMERICANA LEAF 6 [hp_X]/mL
- ARNICA MONTANA 6 [hp_X]/mL
- BISMUTH SUBNITRATE 12 [hp_X]/mL
- CALCIUM FLUORIDE 12 [hp_X]/mL
- CALCIUM SULFIDE 12 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/mL
- DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL
- HELIANTHEMUM CANADENSE 6 [hp_X]/mL
- MERCURY 12 [hp_X]/mL
- MYRRH 8 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
- SODIUM CHLORIDE 3 [hp_X]/mL
- WOOD CREOSOTE 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals
- 43742-1509 - Gum Therapy
- 43742-1509-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-1509 - Gum Therapy
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 43742-1509-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Gum Therapy, a human over the counter drug labeled by Deseret Biologicals. This liquid is formulated for oral use and contains aconitum napellus; agave americana leaf; arnica montana; bismuth subnitrate; calcium fluoride; calcium sulfide; calendula officinalis flowering top; dibasic potassium phosphate; helianthemum canadense; mercury; myrrh; sepia officinalis juice; sodium chloride; wood creosote 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 on August 20, 2019.
How is this Deseret Biologicals product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742150901. 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.