What is NDC 72235-5838?

72235-5838 is the product NDC for Lubracane, Menthol .24 mg/mL gel, listed with the FDA by Ozeion LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Ozeion LLC, NDC labeler code 72235. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lubracane?

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.

Lubracane NDC 72235-5838 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72235-5838Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72235-5838Add 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
72235-5838-1	72235583801	118.3 mL in 1 JAR (72235-5838-1)Marketed from Jan 15, 2018

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): Lubracane
Generic name (nonproprietary): lubracane
Active ingredients: Menthol — .24 mg/mL
Dosage form: Gel
Route: Topical
Labeler: Ozeion LLCNDC labeler code 72235
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 341
Marketing start: Jan 15, 2018
Listing expires: Dec 31, 2027
Identifiers: Product ID 72235-5838_a0727e5c-e1ae-4e4c-a757-25e3c5f83a89SPL ID a0727e5c-e1ae-4e4c-a757-25e3c5f83a89SPL set ID 7c503e3e-1987-4027-8a43-12acf2cb548aUNII L7T10EIP3AUPC 0372235000002

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

N472235583801 followed by a unit qualifier and the quantity

Package 72235-5838-01. 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 Jan 10, 2026.

Indications (excerpt from the label)

Uses For the temporary relief of minor aches and pains of muscles and joints associated with arthritis and minor injuries including sprains, strains and bruises.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72235-5838

What is NDC 72235-5838?: 72235-5838 is the product NDC for Lubracane, Menthol .24 mg/mL gel, listed with the FDA by Ozeion LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lubracane.
What is the active ingredient?: Menthol.
Who is the labeler?: Ozeion LLC, NDC labeler code 72235. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lubracane?: 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.