LenzaPro Flex

Product NDC: 70512-013
11-digit product format: 705120013
Labeler code: 70512
Product ID: 70512-013_457278e8-31e5-637e-e063-6394a90a808d
Type: HUMAN OTC DRUG
Nonproprietary name: Lidocaine/Menthol
Dosage form: PATCH
Route: TOPICAL
Labeler: SOLA Pharmaceuticals
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-02-01
Substance: MENTHOL; LIDOCAINE
Active strength: 40; 40 mg/g; mg/g
Pharmacologic classes: Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: LenzaPro Flex
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	40 mg/g
LIDOCAINE	40 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
98PI200987	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2572014	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ba498f1d-460b-f4e6-e053-2995a90a5755	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70512-013-15	LenzaPro Flex	3 in 1 BOX	PATCH	3		7
70512-013-15	LenzaPro Flex	1 g in 1 POUCH	PATCH	1		7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70512-013-15	EA - Each	70512-013	2a3dd89e-8aed-4d3a-b817-bba1f2a0e083	1	2021-04-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70512-013	LENZAPRO FLEX (LIDOCAINE/MENTHOL) PATCH [SOLA PHARMACEUTICALS]	6	Current NDC, Legacy NDC, 2 package rows	20240522_ba498f1d-460b-f4e6-e053-2995a90a5755.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 120 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Alocane Max	LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	Quest Products LLC	0a35ac19-6883-a733-e063-6294a90ad22d	2024-11-05	Warnings	Exact identifier application number: M017
Alocane Plus	LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	Quest Products, Inc.	cfe8114b-df65-064b-e053-2a95a90a33f6	2024-11-05	Warnings	Exact identifier application number: M017
Alocane Botanicals	LIDOCAINE HYDROCHLORIDE	Quest Products, LLC.	02a8e5c7-56f4-eb0d-e063-6294a90a80cd	2024-11-05	Warnings	Exact identifier application number: M017
Alocane Emergency Burn Pads	LIDOCAINE HYDROCHLORIDE	Quest Products, Inc.	fe58bb89-7216-4121-afd3-d1438bdfbfa2	2024-11-05	Warnings	Exact identifier application number: M017
Licefreee AfterLice	PRAMOXINE HCI	Tec Laboratories Inc.	06c4cc42-a215-3949-e063-6394a90a665e	2024-11-05	Warnings	Exact identifier application number: M017
Antibacterial Lidocaine Wound Gel	BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	ASO LLC	cb9505b7-222d-3a24-e053-2a95a90a0b64	2024-11-05	Warnings	Exact identifier application number: M017
TopCare Pain Relieving Analgesic	LIDOCAINE HYDROCHLORIDE	Topco Associates LLC	6b4783e0-1987-4838-9e8c-b95426d62b28	2024-11-05	Warnings	Exact identifier application number: M017
Eagle Green Balm	CAMPHOR MENTHOL	Borden Company (Private) Limited	6f7a796b-a31c-0e60-e053-2a91aa0a022b	2024-11-04	Warnings	Exact identifier application number: M017
Muscular Balm	CAPSAICIN MENTHOL METHYL SALICYLATE	Borden Company (Private) Limited	ed79f14e-6b3d-4bf2-9c34-d019c1ba2582	2024-11-04	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	A-S Medication Solutions	3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e3	2024-11-04	Warnings	Exact identifier application number: M017
Walgreens Ice Blue Pain Relieving Topical Analgesic	MENTHOL, UNSPECIFIED FORM	Walgreen Company	1c0ee442-ffd2-4f6c-aab2-f70e295378ad	2024-11-04	Warnings	Exact identifier application number: M017
Walgreen Cool n Heat Maximum Strength Pain Relieving	MENTHOL, UNSPECIFIED FORM	Walgreen Company	d5c79476-dde8-4a85-8878-bc2ac3a3d70b	2024-11-04	Warnings	Exact identifier application number: M017
LIDOCAINE	LIDOCAINE	STRATUS PHARMACEUTICALS INC	87a4f559-a4f6-4b9f-98de-b55b073a11c6	2024-11-01	Warnings	Exact identifier application number: M017
Walgreens Nerve Pain Relieving Topical Analgesic	LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM	Walgreen Company	83849eca-e02f-4b43-b3a7-b25e987e08a8	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Arnica White	CAMPHOR	Sanvall Enterprises, Inc	192039a2-aed6-821b-e063-6394a90a7f29	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Arnica Reforzada	CAMPHOR	Sanvall Enterprises, Inc	1921a4b1-cd36-195e-e063-6294a90a8793	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Arnica Pain Releiving Roll On with Camphor	CAMPHOR	Sanvall Enterprises, Inc	173db0e2-611f-55b9-e063-6394a90ac987	2024-10-31	Warnings	Exact identifier application number: M017
Sanar Naturals Camphor	CAMPHOR	Sanvall Enterprises, Inc	1921e851-cf83-0bdb-e063-6294a90a357f	2024-10-31	Warnings	Exact identifier application number: M017
cortisone	HYDROCORTISONE	CVS Pharmacy	c766deac-d993-4e48-a5c3-4cfde7338dff	2024-10-31	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving with Lavender Analgesic	LIDOCAINE HYDROCHLORIDE	Walgreen Company	6c7b39c8-5b65-430a-a529-5b6b14adce18	2024-10-31	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
98PI200987	LIDOCAINE	137-58-6	LIDOCAINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2572014	lidocaine HCl 4 % / menthol 4 % Medicated Patch	PSN	ba498f1d-460b-f4e6-e053-2995a90a5755	7
2572014	lidocaine hydrochloride 0.04 MG/MG / menthol 0.04 MG/MG Medicated Patch	SCD	ba498f1d-460b-f4e6-e053-2995a90a5755	7
2572014	lidocaine HCl 4 % / menthol 4 % Medicated Patch	SY	ba498f1d-460b-f4e6-e053-2995a90a5755	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70512-013-15	70512001315	3 POUCH in 1 BOX (70512-013-15) / 1 g in 1 POUCH	3 pouch	2021-02-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
LenzaPro Flex Patch	SOLA Pharmaceuticals	2025-12-08	HUMAN OTC DRUG LABEL	7
LenzaPro Flex Patch	Direct_Rx	2023-08-16	HUMAN OTC DRUG LABEL	3
Transderm IQ	DIRECT RX	2022-10-04	HUMAN OTC DRUG LABEL	8
LidoMet -10 Patch Kit	PLUM VALLEY PHARMA LLC	2021-11-30	HUMAN OTC DRUG LABEL	1
MenthoReal-10 Topical Paint Patch Kit	Forreal Pharmaceuticals	2021-10-06	HUMAN OTC DRUG LABEL	2