Vertigo Syncope Drops 2115 (vertigo syncope drops) NDC 63083-2115

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2115Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2115Add 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
63083-2115-2	63083211502	59 mL in 1 BOTTLE, DROPPER (63083-2115-2)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): Vertigo Syncope Drops 2115Suffix: 2115
Generic name (nonproprietary): vertigo syncope drops
Active ingredients: Arnica montana whole — 3 [hp_X]/59mLCentella asiatica leaf — 3 [hp_X]/59mLPhosphoric acid — 6 [hp_X]/59mLAmbergris — 12 [hp_X]/59mLSilver nitrate — 12 [hp_X]/59mLAnamirta cocculus fruit — 12 [hp_X]/59mLConium maculatum flowering top — 12 [hp_X]/59mLCanis lupus familiaris milk — 12 [hp_X]/59mLTheridion curassavicum — 12 [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
Identifiers: Product ID 63083-2115_a714711b-afd8-4407-81e6-e9cc56420a66SPL ID a714711b-afd8-4407-81e6-e9cc56420a66SPL set ID 6c89d8af-acd9-4b07-b8c7-14490262fe0aUNII O80TY208ZW, 6810070TYD, E4GA8884NN, XTC0D02P6C, 95IT3W8JZE, 3E8XBL6YYK, Q28R5GF371, G39P120JQT, 9Z8D3HEM8L

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

N463083211502 followed by a unit qualifier and the quantity

Package 63083-2115-02. 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 temporary relief of occasional dizziness or lightheadedness, loss of balance, nausea, or vomiting.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)