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Lidotral 3.88% Roll on

NDC 59088-307, Lidocaine HCI, gel, from PureTek Corporation.

Product NDC
59088-307
Status
Listed
Labeler
PureTek Corporation
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-307 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LIDOCAINE HYDROCHLORIDE38.8 mg/g

Pharmacologic classes

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

Package NDCNDC-11Package
59088-307-075908803070785 g in 1 BOTTLE (59088-307-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db1085fe-0a1f-c4cc-e053-2a95a90aa838

Use it

Look up 59088-307 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-307 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-307. 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.