StellaLife VEGA Oral Care Rinse (rinse) NDC 69685-103

NDC codes

FDA NDC Directory

Product NDC (as listed)69685-103Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69685-0103Add 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
69685-103-16	69685010316	1 BOTTLE, PLASTIC in 1 BOX (69685-103-16) / 473 mL in 1 BOTTLE, PLASTICMarketed from Feb 8, 2019

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): StellaLife VEGA Oral Care Rinse
Generic name (nonproprietary): rinse
Active ingredients: Azadirachta indica bark — 1 [hp_X]/mLCalendula officinalis flower — 1 [hp_X]/mLEchinacea purpurea — 1 [hp_X]/mLPlantago major — 1 [hp_X]/mL
Dosage form: Rinse
Route: Dental
Labeler: StellaLife, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 8, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 69685-103_2b3bdbf3-1885-7a2a-e063-6294a90a6d3cSPL ID 2b3bdbf3-1885-7a2a-e063-6294a90a6d3cSPL set ID 46f3b20e-1ed9-0d1e-e054-00144ff88e88UNII G580B439YI, P0M7O4Y7YD, QI7G114Y98, W2469WNO6U

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N469685010316 followed by a unit qualifier and the quantity

Package 69685-0103-16. 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, 2025.

Indications (excerpt from the label)

recovery kit, gel, spray, rinse indications and usage Gel usage Recovery Kit usage Spray usage

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)