Hormone Combination NDC 43742-1518

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1518Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1518Add 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
43742-1518-1	43742151801	30 mL in 1 BOTTLE, DROPPER (43742-1518-1)Marketed from Aug 21, 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): Hormone Combination
Generic name (nonproprietary): acetaldehyde, dopamine hydrochloride, dhea (dehydroepiandrosterone), 7-oxo- dehydroepiandrosterone 3-acetate, folliculinum, oophorinum (suis), cholesterinum, progesterone, testosterone, cortisone aceticum, aldosterone, androsterone, follicle stimulating hormone
Active ingredients: Acetaldehyde — 6 [hp_X]/mLDopamine hydrochloride — 6 [hp_X]/mLPrasterone — 6 [hp_X]/mL7-keto-dehydroepiandrosterone — 6 [hp_X]/mLEstrone — 8 [hp_X]/mLSus scrofa ovary — 8 [hp_X]/mLCholesterol — 8 [hp_X]/mLProgesterone — 8 [hp_X]/mLTestosterone — 8 [hp_X]/mLCortisone acetate — 12 [hp_X]/mLAldosterone — 12 [hp_C]/mLAndrosterone — 12 [hp_C]/mLFollitropin — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 21, 2019
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)Catecholamines (Chemical structure)Corticosteroid Hormone Receptor Agonists (Mechanism)Gonadotropins (Chemical structure)Progesterone (Chemical structure)
Identifiers: Product ID 43742-1518_fea3c464-8d7e-46db-b159-a305956a8618SPL ID fea3c464-8d7e-46db-b159-a305956a8618SPL set ID 22908e3d-492c-4b18-a070-076f99a81314UNII GO1N1ZPR3B, 7L3E358N9L, 459AG36T1B, 2334LJD2E9, 2DI9HA706A, S7YTV04R8O, 97C5T2UQ7J, 4G7DS2Q64Y, 3XMK78S47O, 883WKN7W8X, 4964P6T9RB, C24W7J5D5R, 076WHW89TWUPC 0810151882253
Pharmacologic class: Androgen; Catecholamine; Corticosteroid; Gonadotropin; Progesterone

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

N443742151801 followed by a unit qualifier and the quantity

Package 43742-1518-01. 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 Mar 11, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • andropause symptoms • fluid retention • emotional swings • menstrual problems • food craving • headache • menopause symptoms • irritability 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)