MQ Lidocaine Pain Relief Patch

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: MQ Lidocaine Pain Relief Patch
Generic name: LIDOCAINE PAIN RELIEF PATCH
Manufacturer: Zhengzhou Miaoqi Medical Technology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 5560cdab-cee8-f6ec-e063-6294a90ad024
SPL ID: 5560cdab-cee9-f6ec-e063-6294a90ad024
Version: 1
Effective date: 2026-06-29
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:17

Harmonized routes table
Harmonized routes
TOPICAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MQ Lidocaine Pain Relief Patch	openfda.brand_name
generic name		LIDOCAINE PAIN RELIEF PATCH	openfda.generic_name
manufacturer name		Zhengzhou Miaoqi Medical Technology Co., Ltd.	openfda.manufacturer_name
ndc	package	83781-016-07	openfda.package_ndc
ndc	package	83781-016-06	openfda.package_ndc
ndc	package	83781-016-08	openfda.package_ndc
ndc	package	83781-016-01	openfda.package_ndc
ndc	package	83781-016-03	openfda.package_ndc
ndc	package	83781-016-04	openfda.package_ndc
ndc	package	83781-016-02	openfda.package_ndc
ndc	package	83781-016-05	openfda.package_ndc
ndc	product	83781-016	openfda.product_ndc
ndc11	package	83781001607	derived:openfda.package_ndc
ndc11	package	83781001603	derived:openfda.package_ndc
ndc11	package	83781001606	derived:openfda.package_ndc
ndc11	package	83781001605	derived:openfda.package_ndc
ndc11	package	83781001602	derived:openfda.package_ndc
ndc11	package	83781001608	derived:openfda.package_ndc
ndc11	package	83781001604	derived:openfda.package_ndc
ndc11	package	83781001601	derived:openfda.package_ndc
rxcui		1649008	openfda.rxcui
spl id		5560cdab-cee9-f6ec-e063-6294a90ad024	id
spl set id		5560cdab-cee8-f6ec-e063-6294a90ad024	set_id
unii		98PI200987	openfda.unii
unii		L7T10EIP3A	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings For external use only

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