VertiFree NDC 68703-353

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-353Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0353Add 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
68703-353-80	68703035380	180 TABLET in 1 BOTTLE, GLASS (68703-353-80)Marketed from Dec 25, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): VertiFree
Generic name (nonproprietary): bryonia, cocculus, gesemium, lobelia
Active ingredients: Lobelia inflata — 30 [hp_C]/1801Gelsemium sempervirens root — 30 [hp_C]/1801Anamirta cocculus seed — 30 [hp_C]/1801Bryonia cretica subsp. Dioica root — 30 [hp_C]/1801
Dosage form: Tablet
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 25, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 68703-353_2ab123a4-1040-63f4-e063-6394a90a9babSPL ID 2ab123a4-1040-63f4-e063-6394a90a9babSPL set ID b6c336e9-6b9a-61eb-e053-2995a90a9332UNII 9PP1T3TC5U, 639KR60Q1Q, 810258W28U, 53UB5FH7CXUPC 0810845016407

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

N468703035380 followed by a unit qualifier and the quantity

Package 68703-0353-80. 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 1, 2025.

Indications (excerpt from the label)

Uses* Uses*: Homeopathic remedy for temporary relief of dizziness and nausea. *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)