MQ Pain Relieving 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 Pain Relieving Patch
Generic name: PAIN RELIEVING PATCH
Manufacturer: Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 0978ff22-c357-e266-e063-6394a90a98a4
SPL ID: 3113d5b9-c963-4cbb-e063-6294a90a9188
Version: 2
Effective date: 2025-03-24
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:13

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MQ Pain Relieving Patch	openfda.brand_name
generic name		PAIN RELIEVING PATCH	openfda.generic_name
manufacturer name		Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	openfda.manufacturer_name
ndc	package	83781-006-02	openfda.package_ndc
ndc	package	83781-006-01	openfda.package_ndc
ndc	package	83781-006-03	openfda.package_ndc
ndc	product	83781-006	openfda.product_ndc
ndc11	package	83781000602	derived:openfda.package_ndc
ndc11	package	83781000601	derived:openfda.package_ndc
ndc11	package	83781000603	derived:openfda.package_ndc
spl id		3113d5b9-c963-4cbb-e063-6294a90a9188	id
spl set id		0978ff22-c357-e266-e063-6394a90a98a4	set_id
unii		5TJD82A1ET	openfda.unii
unii		BZ1R15MTK7	openfda.unii
unii		LAV5U5022Y	openfda.unii
unii		9E8X80D2L0	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Warnings For external use only Do not use: ★on wounds or damaged skin ★if you are allergic to aspirin or salicylates. Stop use and ask a doctor if: ★ Conditions worsen. ★ Symptoms persist for more than 7 days. ★Symptoms clear up and occur again within a few days. ★Rash, itching or excessive skin irritation occurs.

Reported adverse events (FAERS/openFDA)#

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