Lidothol NDC 87063-218

NDC codes

FDA NDC Directory

Product NDC (as listed)87063-218Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87063-0218Add 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
87063-218-99	87063021899	1 TUBE in 1 BOX (87063-218-99) / 99.2 g in 1 TUBEMarketed from May 28, 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): Lidothol
Generic name (nonproprietary): lidocaine hcl, menthol
Active ingredients: Menthol — 5 g/100gLidocaine hydrochloride — 4.5 g/100g
Dosage form: Gel
Route: Cutaneous
Labeler: ASCLEMED USA INC.
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Mar 27, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 87063-218_52dcb054-fc11-49cf-e063-6394a90a53d2SPL ID 52dcb054-fc11-49cf-e063-6394a90a53d2SPL set ID 4e2fad18-13f1-4e61-86db-d72102928717RxCUI 2257313UNII L7T10EIP3A, V13007Z41A
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

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

N487063021899 followed by a unit qualifier and the quantity

Package 87063-0218-99. 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 May 28, 2026.

Indications (excerpt from the label)

INDICATION AND USAGE Lidothol Gel is indicated for relief of pain associated with arthritis, backache, cramps, discomfort, neckache, soreness, sprains, strains. It should be applied only to intact skin.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)