VertiFix NDC 70163-0008

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0008Add 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
70163-0008-1	70163000801	1 BLISTER PACK in 1 CARTON (70163-0008-1) / 60 TABLET in 1 BLISTER PACKMarketed from Mar 11, 2026

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): VertiFix
Generic name (nonproprietary): argentum nitricum, bryonia (alba), causticum, cocculus indicus, gelsemium sempervirens, ipecacuanha, nux vomica, petroleum, sulphur, tabacum
Active ingredients: Silver nitrate — 30 [hp_X]/1Bryonia alba root — 30 [hp_X]/1Causticum — 12 [hp_X]/1Anamirta cocculus seed — 6 [hp_X]/1Gelsemium sempervirens root — 12 [hp_X]/1Ipecac — 6 [hp_X]/1Strychnos nux-vomica seed — 6 [hp_X]/1Kerosene — 12 [hp_X]/1Sulfur — 12 [hp_X]/1Tobacco leaf — 6 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: NaturalCare
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 11, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 70163-0008_456fc8b1-a255-4144-961d-73a922afaddaSPL ID 456fc8b1-a255-4144-961d-73a922afaddaSPL set ID 33b00f06-3202-4904-855c-cdfaa93677a4UNII 95IT3W8JZE, T7J046YI2B, DD5FO1WKFU, 810258W28U, 639KR60Q1Q, 62I3C8233L, 269XH13919, 1C89KKC04E, 70FD1KFU70, 6YR2608RSU
Pharmacologic class: Non-Standardized Plant 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

N470163000801 followed by a unit qualifier and the quantity

Package 70163-0008-01. 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 Aug 27, 2026.

Indications (excerpt from the label)

USES: May help temporarily relieve ■ nausea ■ vertigo ■ dizziness ■ motion sickness due to high places, travel or motion* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Individual responses may vary, and this product may not work for everyone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)