NDC codes

FDA NDC Directory
Product NDC (as listed)87063-323Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0323Add 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
87063-323-158706303231515 POUCH in 1 BOX (87063-323-15) / 1 PATCH in 1 POUCH / 1.38 g in 1 PATCHMarketed from Sep 29, 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 ES
Generic name (nonproprietary)
menthol 5%, lidocaine 4%
Active ingredients
Lidocaine — .04 g/gMenthol — .05 g/g
Dosage form
System
Route
Transdermal
Labeler
ASCLEMED USA INC.NDC labeler code 87063
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 87063-323_5c9c1b16-159a-502f-e063-6394a90a5f17SPL ID 5c9c1b16-159a-502f-e063-6394a90a5f17
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 HCPCS code in Med-Code's directory. Transdermal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N487063032315 followed by a unit qualifier and the quantity

Package 87063-0323-15. 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.

About NDC 87063-323

What is NDC 87063-323?
87063-323 is the product NDC for Lidothol ES, Lidocaine .04 g/g; Menthol .05 g/g system, listed with the FDA by ASCLEMED USA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lidothol ES (Menthol 5%, lidocaine 4%).
What is the active ingredient?
Lidocaine, Menthol.
Who is the labeler?
ASCLEMED USA INC., NDC labeler code 87063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lidothol ES?
2 other product NDCs are listed under this name. See all Lidothol ES NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Lidothol ES NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lidothol ESmenthol 5%, lidocaine 4%Lidocaine .04 g/g; Menthol .05 g/gSystemTransdermalAdvanced Rx of Tennessee, LLC80425-056180425-0561-01
Lidothol ESmenthol 5%, lidocaine 4%Lidocaine .04 g/g; Menthol .05 g/gSystemTransdermalClinic Pharma83881-44583881-0445-15

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