lidotral two percent

Generic: lidocaine hydrochloride

Labeler: puretek corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name lidotral two percent
Generic Name lidocaine hydrochloride
Labeler puretek corporation
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 20 mg/mL

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-304
Product ID 59088-304_185d3e09-4006-b032-e063-6294a90a5efe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2024-05-14

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088304
Hyphenated Format 59088-304

Supplemental Identifiers

RxCUI
1010769
UNII
V13007Z41A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lidotral two percent (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE, SPRAY (59088-304-03)
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "185d3e09-4006-b032-e063-6294a90a5efe", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010769"], "spl_set_id": ["185d3e09-4005-b032-e063-6294a90a5efe"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, SPRAY (59088-304-03)", "package_ndc": "59088-304-03", "marketing_start_date": "20240514"}], "brand_name": "Lidotral Two Percent", "product_id": "59088-304_185d3e09-4006-b032-e063-6294a90a5efe", "dosage_form": "SPRAY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-304", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidotral Two Percent", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240514", "listing_expiration_date": "20261231"}