Male Stimulant NDC 43742-1379

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1379Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1379Add 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
43742-1379-1	43742137901	30 mL in 1 BOTTLE, DROPPER (43742-1379-1)Marketed from Sep 5, 2018

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): Male Stimulant
Generic name (nonproprietary): aralia quinquefolia, agnus castus, ascorbicum acidum, caladium seguinum, kali bromatum, cantharis, damiana, funiculus umbilicalis suis, glandula suprarenalis suis, hypophysis suis, orchitinum (suis), prostate (suis), strychninum phosphoricum, conium maculatum, diencephalon (suis), heart (suis), ferrum phosphoricum, magnesia phosphorica, selenium metallicum, zincum metallicum, pineal gland (suis), cortisone aceticum, manganum phosphoricum, lycopodium clavatum, testosterone, morgan gaertner
Active ingredients: American ginseng — 4 [hp_X]/mLChaste tree fruit — 6 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLDieffenbachia seguine whole — 6 [hp_X]/mLPotassium bromide — 6 [hp_X]/mLLytta vesicatoria — 8 [hp_X]/mLTurnera diffusa leafy twig — 8 [hp_X]/mLSus scrofa umbilical cord — 8 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLSus scrofa pituitary gland — 8 [hp_X]/mLSus scrofa testicle — 8 [hp_X]/mLSus scrofa prostate — 8 [hp_X]/mLStrychnine phosphate dihydrate — 8 [hp_X]/mLConium maculatum flowering top — 8 [hp_X]/mLSus scrofa diencephalon — 8 [hp_X]/mLPork heart — 8 [hp_X]/mLFerrosoferric phosphate — 10 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/mLSelenium — 10 [hp_X]/mLZinc — 10 [hp_X]/mLSus scrofa pineal gland — 12 [hp_X]/mLCortisone acetate — 13 [hp_X]/mLManganese phosphate, Dibasic — 20 [hp_X]/mLLycopodium clavatum spore — 28 [hp_X]/mLTestosterone — 30 [hp_X]/mLSalmonella enterica subsp. Enterica serovar enteritidis — 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: Sep 5, 2018
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)Ascorbic Acid (Chemical structure)Corticosteroid Hormone Receptor Agonists (Mechanism)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-1379_14a5096f-1b11-4ef7-a960-412a8e745c6aSPL ID 14a5096f-1b11-4ef7-a960-412a8e745c6aSPL set ID d48437d6-a54f-4e11-bcfb-9e0d5c1e98daUNII 8W75VCV53Q, 433OSF3U8A, PQ6CK8PD0R, 01800C6E6B, OSD78555ZM, 3Q034RO3BT, RQ2CFA7WWJ, 118OYG6W3H, 398IYQ16YV, L0PFEMQ1DT, KM02613O28, O6UD3347K2, TD67SYY51D, Q28R5GF371, 23PJ4252VL, X876KJM95L, 91GQH8I5F7, HF539G9L3Q, H6241UJ22B, J41CSQ7QDS, 050QZ2EDK7, 883WKN7W8X, VZ3U1H7Q5B, C88X29Y479, 3XMK78S47O, Y3V16D4PV4UPC 0810151881386
Pharmacologic class: Androgen; Calculi Dissolution Agent; Corticosteroid; Osmotic Laxative; Paramagnetic Contrast Agent; Vitamin C

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

N443742137901 followed by a unit qualifier and the quantity

Package 43742-1379-01. 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 Apr 15, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • male hormonal support • low libido • fatigue 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)