Ovarian Drops 5017 (ovarian drops) NDC 63083-5017

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5017Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5017Add 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
63083-5017-2	63083501702	59 mL in 1 BOTTLE, DROPPER (63083-5017-2)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): Ovarian Drops 5017Suffix: 5017
Generic name (nonproprietary): ovarian drops
Active ingredients: Viburnum opulus bark — 2 [hp_X]/59mLChaste tree fruit — 3 [hp_X]/59mLAletris farinosa root — 4 [hp_X]/59mLAmaryllis belladonna whole — 4 [hp_X]/59mLDioscorea villosa tuber — 4 [hp_X]/59mLApis mellifera — 5 [hp_X]/59mLBlack cohosh — 6 [hp_X]/59mLBos taurus ovary — 6 [hp_X]/59mLPackera aurea whole — 6 [hp_X]/59mLSus scrofa uterus — 6 [hp_X]/59mLGelsemium sempervirens root — 8 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 10 [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: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)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 63083-5017_0a26cad6-22c4-4b81-9d6e-3b7b74078079SPL ID 0a26cad6-22c4-4b81-9d6e-3b7b74078079SPL set ID 28d864d6-6fb5-4771-bcdd-db9b68403eb3UNII T1UG6H6805, 433OSF3U8A, O021JGR97X, 11B89M58UN, IWY3IWX2G8, 7S82P3R43Z, K73E24S6X9, 66LZN1C747, 5WS1632J8W, 2595C75F1P, 639KR60Q1Q, HF539G9L3Q
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Standardized Insect Venom Allergenic Extract

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

N463083501702 followed by a unit qualifier and the quantity

Package 63083-5017-02. 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 hot flashes, vaginal dryness, decreased sexual desire, back or abdominal pain or cramping, irritability, or poor concentration.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)