What is NDC 72835-511?

72835-511 is the product NDC for Crysalo, Methyl salicylate 11 g/100mL; Menthol 5 g/100mL liquid, listed with the FDA by V2 Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Crysalo (Methyl Salicylate, Menthol).

V2 Pharma, LLC, NDC labeler code 72835. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Crysalo?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Crysalo NDC 72835-511 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72835-511Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72835-0511Add 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
72835-511-01	7283505110172835051101	57 mL in 1 BOTTLE, SPRAY (72835-511-01)Marketed from Aug 21, 2025

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): Crysalo
Generic name (nonproprietary): methyl salicylate, menthol
Active ingredients: Methyl salicylate — 11 g/100mLMenthol — 5 g/100mL
Dosage form: Liquid
Route: Topical
Labeler: V2 Pharma, LLCNDC labeler code 72835
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Aug 21, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 72835-511_8cba42b5-6ae5-410a-aa77-69b2ccd05860SPL ID 8cba42b5-6ae5-410a-aa77-69b2ccd05860SPL set ID d6c475f0-1098-41cd-868a-a5e528a5e5aeRxCUI 2722189UNII LAV5U5022Y, L7T10EIP3A

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

N472835051101 followed by a unit qualifier and the quantity

Package 72835-0511-01. 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 Jul 6, 2026.

Indications (excerpt from the label)

Uses Temporary relief of minor aches and pains associated with: Simple backache Arthritis Strains, sprains, and bruises

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72835-511

What is NDC 72835-511?: 72835-511 is the product NDC for Crysalo, Methyl salicylate 11 g/100mL; Menthol 5 g/100mL liquid, listed with the FDA by V2 Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Crysalo (Methyl Salicylate, Menthol).
What is the active ingredient?: Methyl salicylate, Menthol.
Who is the labeler?: V2 Pharma, LLC, NDC labeler code 72835. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Crysalo?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Crysalo (Methyl salicylate, menthol) NDC 72835-511