Hormone Harmony NDC 70558-0008

NDC codes

FDA NDC Directory

Product NDC (as listed)70558-0008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70558-0008Add 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
70558-0008-1	70558000801	30 mL in 1 BOTTLE, DROPPER (70558-0008-1)Marketed from Oct 12, 2020

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 Harmony
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 — 8 [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: Pro Weight Loss Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 12, 2020
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 70558-0008_8c95390f-f204-41d4-a7c8-22a37a5a04efSPL ID 8c95390f-f204-41d4-a7c8-22a37a5a04efSPL set ID 123f5269-45eb-4dcd-be66-76c6665b8d13UNII GO1N1ZPR3B, 7L3E358N9L, 459AG36T1B, 2334LJD2E9, 2DI9HA706A, S7YTV04R8O, 97C5T2UQ7J, 4G7DS2Q64Y, 3XMK78S47O, 883WKN7W8X, 4964P6T9RB, C24W7J5D5R, 076WHW89TW
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

N470558000801 followed by a unit qualifier and the quantity

Package 70558-0008-01. 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 22, 2024.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: Temporary relief of symptoms related to hormone imbalances of insufficiencies in men and women, including low energy, inability to handle stress, trouble focusing, changes in mood, infertility, irregular menstrual cycles (females), and lack of libido.** **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)