MQ Motion 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 Motion Patch
Generic name: MOTION PATCH
Manufacturer: Zhengzhou Miaoqi Medical Technology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 3a70bc22-8e31-2d4c-e063-6394a90a3b24
SPL ID: 3a70bc22-8e32-2d4c-e063-6394a90a3b24
Version: 1
Effective date: 2025-07-21
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:55:50

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M009	openfda.application_number
brand name		MQ Motion Patch	openfda.brand_name
generic name		MOTION PATCH	openfda.generic_name
manufacturer name		Zhengzhou Miaoqi Medical Technology Co., Ltd.	openfda.manufacturer_name
ndc	package	83781-012-06	openfda.package_ndc
ndc	package	83781-012-02	openfda.package_ndc
ndc	package	83781-012-03	openfda.package_ndc
ndc	package	83781-012-08	openfda.package_ndc
ndc	package	83781-012-04	openfda.package_ndc
ndc	package	83781-012-07	openfda.package_ndc
ndc	package	83781-012-01	openfda.package_ndc
ndc	package	83781-012-05	openfda.package_ndc
ndc	product	83781-012	openfda.product_ndc
ndc11	package	83781001201	derived:openfda.package_ndc
ndc11	package	83781001207	derived:openfda.package_ndc
ndc11	package	83781001203	derived:openfda.package_ndc
ndc11	package	83781001205	derived:openfda.package_ndc
ndc11	package	83781001202	derived:openfda.package_ndc
ndc11	package	83781001206	derived:openfda.package_ndc
ndc11	package	83781001204	derived:openfda.package_ndc
ndc11	package	83781001208	derived:openfda.package_ndc
spl id		3a70bc22-8e32-2d4c-e063-6394a90a3b24	id
spl set id		3a70bc22-8e31-2d4c-e063-6394a90a3b24	set_id
unii		L7T10EIP3A	openfda.unii
unii		C5529G5JPQ	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 Pregnant women, breastfeeding mothers,children under the age of 4 should not use.Do not use if the skin has abnormalities, wounds, eczema, inflammation, allergies.Please keep it out of reach of children and pets.For external use only.

Reported adverse events (FAERS/openFDA)#

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