lenzapro flex

Generic: lidocaine/menthol

Labeler: sola pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lenzapro flex
Generic Name lidocaine/menthol
Labeler sola pharmaceuticals
Dosage Form PATCH
Routes
TOPICAL
Active Ingredients

lidocaine 40 mg/g, menthol 40 mg/g

Manufacturer
SOLA Pharmaceuticals

Identifiers & Regulatory

Product NDC 70512-013
Product ID 70512-013_457278e8-31e5-637e-e063-6394a90a808d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2021-02-01

Pharmacologic Class

Established (EPC)
amide local anesthetic [epc] antiarrhythmic [epc]
Chemical Structure
amides [cs]
Physiologic Effect
local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70512013
Hyphenated Format 70512-013

Supplemental Identifiers

RxCUI
2572014
UPC
0070512013157
UNII
98PI200987 L7T10EIP3A
NUI
N0000175682 M0000897 N0000175426 N0000175976

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 lenzapro flex (source: ndc)
Generic Name lidocaine/menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/g
source: ndc
Packaging
  • 3 POUCH in 1 BOX (70512-013-15) / 1 g in 1 POUCH
source: ndc

Packages (1)

Ingredients (2)

lidocaine (40 mg/g) menthol (40 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "457278e8-31e5-637e-e063-6394a90a808d", "openfda": {"nui": ["N0000175682", "M0000897", "N0000175426", "N0000175976"], "upc": ["0070512013157"], "unii": ["98PI200987", "L7T10EIP3A"], "rxcui": ["2572014"], "spl_set_id": ["ba498f1d-460b-f4e6-e053-2995a90a5755"], "pharm_class_cs": ["Amides [CS]"], "pharm_class_pe": ["Local Anesthesia [PE]"], "pharm_class_epc": ["Amide Local Anesthetic [EPC]", "Antiarrhythmic [EPC]"], "manufacturer_name": ["SOLA Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 BOX (70512-013-15)  / 1 g in 1 POUCH", "package_ndc": "70512-013-15", "marketing_start_date": "20210201"}], "brand_name": "LenzaPro Flex", "product_id": "70512-013_457278e8-31e5-637e-e063-6394a90a808d", "dosage_form": "PATCH", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "70512-013", "generic_name": "Lidocaine/Menthol", "labeler_name": "SOLA Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LenzaPro Flex", "active_ingredients": [{"name": "LIDOCAINE", "strength": "40 mg/g"}, {"name": "MENTHOL", "strength": "40 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}