Prostate NDC 43742-2092

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2092Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2092Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43742-2092-1	43742209201	30 mL in 1 BOTTLE, DROPPER (43742-2092-1)Marketed from Oct 11, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Prostate
Generic name (nonproprietary): 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)
Active ingredients: Petroselinum crispum whole — 4 [hp_X]/mLPopulus tremuloides bark — 4 [hp_X]/mLPopulus tremuloides leaf — 4 [hp_X]/mLSaw palmetto — 4 [hp_X]/mLChimaphila umbellata whole — 5 [hp_X]/mLAdenosine triphosphate disodium — 6 [hp_X]/mLEquol — 6 [hp_X]/mLWood creosote — 6 [hp_X]/mLNadide — 6 [hp_X]/mLTestosterone — 6 [hp_X]/mLSus scrofa prostate — 8 [hp_X]/mLSuccinic acid — 8 [hp_X]/mLCalcium sulfide — 10 [hp_X]/mLConium maculatum flowering top — 30 [hp_X]/mLProteus mirabilis — 30 [hp_C]/mLProteus vulgaris — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 11, 2023
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)
Identifiers: Product ID 43742-2092_05ad47b4-7738-4310-8c64-fea248ad289bSPL ID 05ad47b4-7738-4310-8c64-fea248ad289bSPL set ID 776af24a-d9c1-4ecd-8e5d-0ab32c60e715UNII 1WZA4Y92EX, 5543O0CEID, 7IIH57D9E0, J7WWH9M8QS, WCK21A9W9J, 5L51B4DR1G, 2T6D2HPX7Q, 3JYG22FD73, 0U46U6E8UK, 3XMK78S47O, O6UD3347K2, AB6MNQ6J6L, 1MBW07J51Q, Q28R5GF371, C177VR41DV, 11T9HCO30OUPC 0810151881799
Pharmacologic class: Androgen

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742209201 followed by a unit qualifier and the quantity

Package 43742-2092-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Aug 19, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of the symptoms including: • prostate support • weak urine stream • frequent urination These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)