NDC codes

FDA NDC Directory
Product NDC (as listed)69685-173Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69685-0173Add 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 NDC11-digit (billing)PackageCopy
69685-173-16696850173161 BOTTLE, PLASTIC in 1 BOX (69685-173-16) / 473 mL in 1 BOTTLE, PLASTICMarketed from Sep 1, 2026

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 Vanilla Mint Professional FormulaSuffix: Professional Formula
Generic name (nonproprietary)
azadirachta indica, calendula, echinacea purpurea, plantago major
Active ingredients
Plantago major — 3 [hp_X]/mLAzadirachta indica bark — 3 [hp_X]/mLEchinacea purpurea — 3 [hp_X]/mLCalendula officinalis flower — 3 [hp_X]/mL
Dosage form
Rinse
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 69685-173_5b39cde7-68be-12ba-e063-6294a90a24c9SPL ID 5b39cde7-68be-12ba-e063-6294a90a24c9

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

N469685017316 followed by a unit qualifier and the quantity

Package 69685-0173-16. 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

The FDA listing for this product does not reference a label (SPL) set.

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NDC 69685-173 | Med-Code