Zhuang Gu Feng Shi 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#

ProductZhuang Gu Feng Shi Pain Relieving Plaster
Active ingredientMETHYL SALICYLATE, CAMPHOR (NATURAL), MENTHOL
Label structure11 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: 12%...External Analgesic

Camphor: 3.8%....External Analgesic

Menthol: 2.6%....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.

Ask a doctor or pharmacist before use if:

OTC - ASK DOCTOR/PHARMACIST SECTION

You are allergic to salicylates or asprin.

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, angelica dahurica root, atractylodes lancea root, angelica sinensis root, anise, ephedra sinica stem, natural latex rubber

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package
package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1550967camphor 3.8 % / menthol 2.6 % / methyl salicylate 12 % Medicated PatchPSN2
1550967camphor 0.038 MG/MG / menthol 0.026 MG/MG / methyl salicylate 0.12 MG/MG Medicated PatchSCD2
1550967camphor 3.8 % / menthol 2.6 % / methyl salicylate 12 % Medicated PatchSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1286903544055175package.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51367-022-08Zhuang Gu Feng Shi Pain Relieving Plaster8 in 1 PACKAGEPLASTER82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51367-022ZHUANG GU FENG SHI PAIN RELIEVING PLASTER (METHYL SALICYLATE, CAMPHOR, MENTHOL) PLASTER [INTERNATIONAL NATURE NUTRACEUTICALS]2Legacy NDC, 1 package rows20170731_529c7d42-d3be-4403-9e8f-770f08fe18bf.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
ANGELICA DAHURICA ROOTINACTIVE INGREDIENT1V63N2S9721
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG1
ANISEINACTIVE INGREDIENT21C2F5E8RE1
ATRACTYLODES LANCEA ROOTINACTIVE INGREDIENTCAZ6282J2O1
EPHEDRA SINICA STEMINACTIVE INGREDIENT55L3XLO37E1
GINGERINACTIVE INGREDIENTC5529G5JPQ1
KAEMPFERIA GALANGA ROOTINACTIVE INGREDIENT7B7U9D12AI1
NATURAL LATEX RUBBERINACTIVE INGREDIENT2LQ0UUW8IN1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51367-02251367-022-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GINGERGINGERC5529G5JPQSYRUP / ORAL0.05 ml/5mlExact identifier — unii candidate
2 equally ranked IID candidates
ANISEANISE21C2F5E8REELIXIR / ORAL0.15 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates
GINGERGINGERC5529G5JPQELIXIR / ORAL10 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates
ANISEANISE21C2F5E8RESOLUTION / ORAL72 mgExact 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
6c46aa16-7dfc-43c9-a1e1-ac124e68287e529c7d42-d3be-4403-9e8f-770f08fe18bf2017-07-31WarningsExact identifier
spl id: 6c46aa16-7dfc-43c9-a1e1-ac124e68287e
spl set id: 529c7d42-d3be-4403-9e8f-770f08fe18bf

Reported adverse events (FAERS/openFDA)#

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