lidoease 2%

Generic: lidocaine hcl 2%

Labeler: puretek corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lidoease 2%
Generic Name lidocaine hcl 2%
Labeler puretek corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 20 mg/g

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-221
Product ID 59088-221_3ba0c0ff-0f7b-7a29-e063-6294a90a547a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-08-06

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 59088221
Hyphenated Format 59088-221

Supplemental Identifiers

RxCUI
1011852
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 lidoease 2% (source: ndc)
Generic Name lidocaine hcl 2% (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 85 g in 1 TUBE (59088-221-07)
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride (20 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3ba0c0ff-0f7b-7a29-e063-6294a90a547a", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1011852"], "spl_set_id": ["3ba0c0ff-0f7a-7a29-e063-6294a90a547a"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 TUBE (59088-221-07)", "package_ndc": "59088-221-07", "marketing_start_date": "20250806"}], "brand_name": "Lidoease 2%", "product_id": "59088-221_3ba0c0ff-0f7b-7a29-e063-6294a90a547a", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-221", "generic_name": "Lidocaine HCl 2%", "labeler_name": "PureTek Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lidoease 2%", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}