Prostate Liquid
NDC Package 43742-2092-1
Package Information
Prostate (petroselinum sativum, populus tremuloides, sabal serrulata, chimaphila umbellata, adenosinum triphosphoricum dinatrum, equol, kreosotum, nadidum, testosterone, prostate (suis), succinicum acidum, hepar sulphuris calcareum, conium maculatum, proteus (mirabilis), proteus (vulgaris)) liquids is 1-10 drops under the tongue, 2 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2092.
Identification & Billing
Clinical Specifications
- PETROSELINUM CRISPUM WHOLE 6 [hp_X]/mL
- POPULUS TREMULOIDES BARK 10 [hp_X]/mL
- POPULUS TREMULOIDES LEAF 5 [hp_X]/mL
- SAW PALMETTO 30 [hp_X]/mL
- CHIMAPHILA UMBELLATA WHOLE 6 [hp_X]/mL
- ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
- EQUOL 4 [hp_X]/mL
- WOOD CREOSOTE 4 [hp_X]/mL
- NADIDE 4 [hp_X]/mL
- TESTOSTERONE 30 [hp_C]/mL
- SUS SCROFA PROSTATE 30 [hp_C]/mL
- SUCCINIC ACID 4 [hp_X]/mL
- CALCIUM SULFIDE 8 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/mL
- PROTEUS MIRABILIS 6 [hp_X]/mL
- PROTEUS VULGARIS 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-2092 - Prostate
- 43742-2092-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-2092 - Prostate
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43742-2092-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Prostate, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains petroselinum crispum whole; populus tremuloides bark; populus tremuloides leaf; saw palmetto; chimaphila umbellata whole; adenosine triphosphate disodium; equol; wood creosote; nadide; testosterone; sus scrofa prostate; succinic acid; calcium sulfide; conium maculatum flowering top; proteus mirabilis; proteus vulgaris 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 October 11, 2023. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742209201. 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.