dermacinrx lidotral

Generic: lidocaine hydrochloride

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

Drug Facts

Product Profile

Brand Name dermacinrx lidotral
Generic Name lidocaine hydrochloride
Labeler puretek corporation
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 38.8 mg/g

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-371
Product ID 59088-371_36a4cb7d-d1e8-4056-8344-c9f110820fcc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2015-12-03

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 59088371
Hyphenated Format 59088-371

Supplemental Identifiers

RxCUI
1723991 1723996
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 dermacinrx lidotral (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 38.8 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (59088-371-07) / 85 g in 1 TUBE
source: ndc

Packages (1)

59088-371-07 1 TUBE in 1 CARTON (59088-371-07) / 85 g in 1 TUBE

Ingredients (1)

lidocaine hydrochloride (38.8 mg/g)

Linked Drug Pages (1)

DermacinRx Lidotral ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "36a4cb7d-d1e8-4056-8344-c9f110820fcc", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1723991", "1723996"], "spl_set_id": ["23efec58-67cc-418d-85f5-7ef156443cbf"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59088-371-07)  / 85 g in 1 TUBE", "package_ndc": "59088-371-07", "marketing_start_date": "20151203"}], "brand_name": "DermacinRx Lidotral", "product_id": "59088-371_36a4cb7d-d1e8-4056-8344-c9f110820fcc", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-371", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DermacinRx Lidotral", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20151203", "listing_expiration_date": "20261231"}