bruselix gel

Generic: lidocaine hci 3.88%

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

Drug Facts

Product Profile

Brand Name bruselix gel
Generic Name lidocaine hci 3.88%
Labeler puretek corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 38.8 mg/g

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-233
Product ID 59088-233_155d0c2a-6027-c589-e063-6394a90a07dd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2024-03-21

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 59088233
Hyphenated Format 59088-233

Supplemental Identifiers

RxCUI
2675768 2678305
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 bruselix gel (source: ndc)
Generic Name lidocaine hci 3.88% (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 38.8 mg/g
source: ndc
Packaging
  • 57 g in 1 TUBE (59088-233-05)
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride (38.8 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "155d0c2a-6027-c589-e063-6394a90a07dd", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["2675768", "2678305"], "spl_set_id": ["1420ec27-64f3-9117-e063-6294a90a8ece"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "57 g in 1 TUBE (59088-233-05)", "package_ndc": "59088-233-05", "marketing_start_date": "20240321"}], "brand_name": "Bruselix Gel", "product_id": "59088-233_155d0c2a-6027-c589-e063-6394a90a07dd", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-233", "generic_name": "Lidocaine HCI 3.88%", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bruselix Gel", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}