Fem Pro Drops 2025 (fem pro drops) NDC 63083-2025

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2025Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2025Add 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
63083-2025-2	63083202502	59 mL in 1 BOTTLE, DROPPER (63083-2025-2)Marketed from Aug 15, 1985

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): Fem Pro Drops 2025Suffix: 2025
Generic name (nonproprietary): fem pro drops
Active ingredients: Chaste tree fruit — 3 [hp_X]/59mLCaulophyllum thalictroides root — 6 [hp_X]/59mLBlack cohosh — 6 [hp_X]/59mLRubus idaeus fruit volatile oil — 6 [hp_X]/59mLBos taurus pituitary gland, Posterior — 12 [hp_X]/59mLBeta-endorphin human — 30 [hp_X]/59mLEstrogens, Conjugated — 30 [hp_X]/59mLProgesterone — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Estrogen Receptor Agonists (Mechanism)Conjugated (USP) (Chemical structure)Progesterone (Chemical structure)
Identifiers: Product ID 63083-2025_61f3ee5d-927e-45dd-a953-486b76904404SPL ID 61f3ee5d-927e-45dd-a953-486b76904404SPL set ID e90ddaec-fc0e-4277-9cc6-6d3973d8e1eeUNII 433OSF3U8A, JTJ6HH6YEH, K73E24S6X9, 276X2YNL0K, 7JM57I419K, 3S51P4W3XQ, IU5QR144QX, 4G7DS2Q64Y
Pharmacologic class: Estrogen; 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

N463083202502 followed by a unit qualifier and the quantity

Package 63083-2025-02. 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 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of painful or heavy menses, abdominal cramping, or backache.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)