CHINESE RED TIGER Plaster

Manufacturer
Guangzhou Su Mai Feng International Trading Co., Ltd.
Effective date
2025-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:45

Label at a glance#

ProductCHINESE RED TIGER Plaster
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

Temporarily relieves musclesoreness and minor joint spainrelated to: sprains backache strains

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION


Do not apply to wounds or damaged skin
Do not use with other ointments,creams, sprays, or liniments
Do not bandage or use with heating pad or device
Store in a cool dry place away fromdireet sunlight

OTC - WHEN USING SECTION


When using this product:
Use only as directed
Avoid contact with eyes or mucous membranes

OTC - STOP USE SECTION


lf swelling, blistering or other discomfortoccurs, please stop using it and consult your doctor immediately.
lf symptoms have not been relieved after using this product for more than 7 days, please stop using it and consult your doctor immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed accidentally , get medica help or contact with Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION


Clean and dry the affected area and remove a patch from its packaging. Partially peel back the protective film and apply the exposed part of the patch to the site of pain.
Carefully remove remaining film while pressing the patch firmly on the skin. Leave the patch in place forup to 8 hours.

INACTIVE INGREDIENT SECTION

Mugwort, osmanthus Oil, Mentha Oil,Eucalyptus Oil, Cinnamon, Safflower,Myrrh.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84198-00884198-008-01, 84198-008-08, 84198-008-64

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
44a4c550-cbe6-ec67-e063-6294a90accf53dba7ca2-83fd-4c2b-e063-6294a90a95712025-11-28WarningsExact identifier
spl set id: 3dba7ca2-83fd-4c2b-e063-6294a90a9571

Reported adverse events (FAERS/openFDA)#

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