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Lidothol ES

NDC 87063-323, menthol 5%, lidocaine 4%, system, from ASCLEMED USA INC..

Product NDC
87063-323
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
SYSTEM
Route
TRANSDERMAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-323 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LIDOCAINE.04 g/g
  • MENTHOL.05 g/g

Pharmacologic classes

Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]

Package NDCNDC-11Package
87063-323-158706303231515 POUCH in 1 BOX (87063-323-15) / 1 PATCH in 1 POUCH / 1.38 g in 1 PATCH

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/107eed24-d1a5-429e-b388-fad8879e9ca4

Use it

Look up 87063-323 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-323 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-323. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.