FDA.reportPublic FDA data

Refined Gou Pi Pain Relieving Plaster

Manufacturer
International Nature Nutraceuticals | Huangshi Hygienic Material Medicine Co., Ltd
Effective date
2017-07-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:52:05

Label at a glance#

ProductRefined Gou Pi Pain Relieving Plaster
Active ingredientMETHYL SALICYLATE, CAMPHOR (NATURAL), MENTHOL
Label structure10 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: simple backache, arthritis, strains, bruises, strains

Dosage and administration

Adults and children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 8 hours. Children 2 to 12 years of age and adults with compromised health: use only under the guidance of a doctor Children under 2 years of age: do not use.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate: 14.6%...External Analgesic

Camphor: 3.5%....External Analgesic

Menthol: 2.3%....Extermal Analgesic

Uses:

OTC - PURPOSE SECTION

For the temporary relief of minor aches and pains of muscles and joints due to: simple backache, arthritis, strains, bruises, strains

Warnings:

WARNINGS SECTION

For external use only

When Using this product:

OTC - DO NOT USE SECTION

Avoid contact with the eyes. Do not apply to wounds or damaged skin. Do not bandage tightly.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case swallowed, get medical help or contact a poison control center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 8 hours.

Children 2 to 12 years of age and adults with compromised health: use only under the guidance of a doctor

Children under 2 years of age: do not use.

Storage

INDICATIONS & USAGE SECTION

Store at 15°C to 30°C (59°F to 86°F)

Keep away from heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Kaemferia galanga root, ginger, corydalis yanhusuo tuber, paprika, stephania root, impatiens balsamina leaf, natural latex rubber

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1547758camphor 3.5 % / menthol 2.3 % / methyl salicylate 14.6 % Medicated PatchPSN2
1547758camphor 0.035 MG/MG / menthol 0.023 MG/MG / methyl salicylate 0.146 MG/MG Medicated PatchSCD2
1547758camphor 3.5 % / menthol 2.3 % / methyl salicylate 14.6 % Medicated PatchSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1286903544055113package.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51367-020-04Refined Gou Pi Pain Relieving Plaster8 in 1 PACKAGEPLASTER82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51367-020REFINED GOU PI PAIN RELIEVING PLASTER (METHYL SALICYLATE, CAMPHOR, MENTHOL) PLASTER [INTERNATIONAL NATURE NUTRACEUTICALS]2Legacy NDC, 1 package rows20170731_3670a007-b3d0-43e2-9d22-284e4c65d682.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9411
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9411
MENTHOLACTIVE MOIETYL7T10EIP3A1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
CORYDALIS YANHUSUO TUBERINACTIVE INGREDIENT0TUP42692Z1
GINGERINACTIVE INGREDIENTC5529G5JPQ1
IMPATIENS BALSAMINA LEAFINACTIVE INGREDIENTLH9E1X602V1
KAEMPFERIA GALANGA ROOTINACTIVE INGREDIENT7B7U9D12AI1
NATURAL LATEX RUBBERINACTIVE INGREDIENT2LQ0UUW8IN1
PAPRIKAINACTIVE INGREDIENTX72Z47861V1
STEPHANIA TETRANDRA ROOTINACTIVE INGREDIENT48PS81XHK01

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51367-02051367-020-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYL SALICYLATELAV5U5022YACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB
KAEMPFERIA GALANGA ROOT7B7U9D12AIIACT
GINGERC5529G5JPQIACT
CORYDALIS YANHUSUO TUBER0TUP42692ZIACT
PAPRIKAX72Z47861VIACT
STEPHANIA TETRANDRA ROOT48PS81XHK0IACT
IMPATIENS BALSAMINA LEAFLH9E1X602VIACT
NATURAL LATEX RUBBER2LQ0UUW8INIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GINGERGINGERC5529G5JPQELIXIR / ORAL10 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates
GINGERGINGERC5529G5JPQSYRUP / ORAL0.05 ml/5mlExact identifier — unii candidate
2 equally ranked IID candidates

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
e6363226-3b02-4c5b-85cd-26076facd17b3670a007-b3d0-43e2-9d22-284e4c65d6822017-07-31WarningsExact identifier
spl id: e6363226-3b02-4c5b-85cd-26076facd17b
spl set id: 3670a007-b3d0-43e2-9d22-284e4c65d682

Reported adverse events (FAERS/openFDA)#

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