Dendracin Neurodendraxcin NDC 68788-7696

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7696Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7696Add 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
68788-7696-1	68788769601	120 mL in 1 BOTTLE (68788-7696-1)Marketed from Apr 1, 2020
68788-7696-6	68788769606	60 mL in 1 BOTTLE (68788-7696-6)Marketed from Apr 1, 2020

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): Dendracin Neurodendraxcin
Generic name (nonproprietary): methyl salicylate, menthol and capsaicin
Active ingredients: Methyl salicylate — 18 g/60mLMenthol, Unspecified form — 6 g/60mLCapsaicin — .015 g/60mL
Dosage form: Lotion
Route: Topical
Labeler: Preferred Pharmaceuticals, Inc.
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication MO 17
Marketing start: Apr 1, 2020
Listing expires: Dec 31, 2027
Identifiers: Product ID 68788-7696_6aab2cb8-6f5c-4bb1-a7ac-01192d18956dSPL ID 6aab2cb8-6f5c-4bb1-a7ac-01192d18956dSPL set ID 43a8f9c1-6cf1-4f27-9995-4f0ce08971daRxCUI 1116967, 1116971UNII LAV5U5022Y, L7T10EIP3A, S07O44R1ZM

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468788769601 followed by a unit qualifier and the quantity

Package 68788-7696-01. 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 Apr 1, 2026.

Indications (excerpt from the label)

USES: For temporary relief of mild pain due to muscular strain, arthritis, and simple back pain. Does not cure any disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)