Dizzy Formula NDC 83027-0001

NDC codes

FDA NDC Directory

Product NDC (as listed)83027-0001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83027-0001Add 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
83027-0001-1	83027000101	60 mL in 1 BOTTLE, SPRAY (83027-0001-1)Marketed from Feb 20, 2023

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): Dizzy Formula
Generic name (nonproprietary): arnica montana, hydrocotyle asiatica, ambra grisea, argentum nitricum, cocculus indicus, conium maculatum, lac caninum, theridion
Active ingredients: Arnica montana whole — 3 [hp_X]/mLCentella asiatica flowering top — 3 [hp_X]/mLAmbergris — 12 [hp_X]/mLSilver nitrate — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLCanis lupus familiaris milk — 12 [hp_X]/mLTheridion curassavicum — 18 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Nutritional Specialties, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 20, 2023
Listing expires: Dec 31, 2027
Identifiers: Product ID 83027-0001_bc927253-1a40-44ad-8ef5-46240f498cf0SPL ID bc927253-1a40-44ad-8ef5-46240f498cf0SPL set ID aaccfd13-6559-4976-90d1-aa3b4a4a79dbUNII O80TY208ZW, J02K2IV2PB, XTC0D02P6C, 95IT3W8JZE, 810258W28U, Q28R5GF371, G39P120JQT, 9Z8D3HEM8LUPC 0649818031150

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

N483027000101 followed by a unit qualifier and the quantity

Package 83027-0001-01. 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 31, 2026.

Indications (excerpt from the label)

USES: For temporary relief of •dizziness, •light headedness, and •sensations of motion or spinning.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)