MQUPIN TIGER 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: MQUPIN TIGER Patch
Generic name: TIGER PATCH
Manufacturer: Zhengzhou Miaoqi Medical Technology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 5977cbb5-94c7-cb24-e063-6294a90a2e07
SPL ID: 5977cbb5-94c8-cb24-e063-6294a90a2e07
Version: 1
Effective date: 2026-08-20
Source export date: 2026-10-27
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:50:30

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MQUPIN TIGER Patch	openfda.brand_name
generic name		TIGER PATCH	openfda.generic_name
manufacturer name		Zhengzhou Miaoqi Medical Technology Co., Ltd.	openfda.manufacturer_name
ndc	package	83781-017-03	openfda.package_ndc
ndc	package	83781-017-01	openfda.package_ndc
ndc	package	83781-017-06	openfda.package_ndc
ndc	package	83781-017-05	openfda.package_ndc
ndc	package	83781-017-04	openfda.package_ndc
ndc	package	83781-017-02	openfda.package_ndc
ndc	product	83781-017	openfda.product_ndc
ndc11	package	83781001706	derived:openfda.package_ndc
ndc11	package	83781001704	derived:openfda.package_ndc
ndc11	package	83781001705	derived:openfda.package_ndc
ndc11	package	83781001703	derived:openfda.package_ndc
ndc11	package	83781001701	derived:openfda.package_ndc
ndc11	package	83781001702	derived:openfda.package_ndc
spl id		5977cbb5-94c8-cb24-e063-6294a90a2e07	id
spl set id		5977cbb5-94c7-cb24-e063-6294a90a2e07	set_id
unii		213N3S8275	openfda.unii
unii		M89NIB437X	openfda.unii
unii		L7T10EIP3A	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 For single use only. Do not swallow. Do not use on allergic skin and wounds. This product is not a substitute for medicine. Stop use if skin irritation such as rash, or redness occurs. Stop use and ask a doctor if conditions worsen.

Reported adverse events (FAERS/openFDA)#

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