What is NDC 43742-1585?

43742-1585 is the product NDC for Gyno Complex, Viburnum opulus bark 3 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gyno Complex (Viburnum Opulus, Magnesia Phosphorica, Folliculinum, Pulsatilla (Pratensis), Borax, Mercurius Solubilis, Nitricum Acidum, Silicea, Thuja Occidentalis).

What is the active ingredient?

Viburnum opulus bark, Magnesium phosphate, Dibasic trihydrate, Estrone, Anemone pratensis, Sodium borate, Mercurius solubilis, Nitric acid, Silicon dioxide, Thuja occidentalis leaf.

Deseret Biologicals, Inc, NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gyno Complex?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gyno Complex NDC 43742-1585 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1585Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1585Add 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
43742-1585-1	4374215850143742158501	30 mL in 1 BOTTLE, DROPPER (43742-1585-1)Marketed from Oct 10, 2019

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): Gyno Complex
Generic name (nonproprietary): viburnum opulus, magnesia phosphorica, folliculinum, pulsatilla (pratensis), borax, mercurius solubilis, nitricum acidum, silicea, thuja occidentalis
Active ingredients: Viburnum opulus bark — 3 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 8 [hp_X]/mLEstrone — 12 [hp_X]/mLAnemone pratensis — 12 [hp_X]/mLSodium borate — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLNitric acid — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLThuja occidentalis leaf — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, IncNDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 10, 2019
Listing expires: Dec 31, 2026
Other FDA classes: 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)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-1585_4a0ff05b-b051-4fe0-8a3d-4eb136735a5cSPL ID 4a0ff05b-b051-4fe0-8a3d-4eb136735a5cSPL set ID dfaaa56a-4226-4f62-a219-d3f89fe7afe3UNII T1UG6H6805, HF539G9L3Q, 2DI9HA706A, 8E272251DI, 91MBZ8H3QO, 324Y4038G2, 411VRN1TV4, ETJ7Z6XBU4, 0T0DQN8786
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N443742158501 followed by a unit qualifier and the quantity

Package 43742-1585-01. 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 Jan 12, 2023.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to hormonal dysfunction including irregular, excessive or absent menstruation, vaginal discharge, pain and fever.** **These statements are based upon traditional 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)

About NDC 43742-1585

What is NDC 43742-1585?: 43742-1585 is the product NDC for Gyno Complex, Viburnum opulus bark 3 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gyno Complex (Viburnum Opulus, Magnesia Phosphorica, Folliculinum, Pulsatilla (Pratensis), Borax, Mercurius Solubilis, Nitricum Acidum, Silicea, Thuja Occidentalis).
What is the active ingredient?: Viburnum opulus bark, Magnesium phosphate, Dibasic trihydrate, Estrone, Anemone pratensis, Sodium borate, Mercurius solubilis, Nitric acid, Silicon dioxide, Thuja occidentalis leaf.
Who is the labeler?: Deseret Biologicals, Inc, NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gyno Complex?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.