FDA.reportPublic FDA data

Shang Shi Zhi Tong Pain Relieving Plaster

Manufacturer
International Nature Nutraceuticals | Huangshi Hygienic Material Medicine Co., Ltd
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:48:06

Label at a glance#

ProductShang Shi Zhi Tong 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: 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.

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

Clove, schizonpeta bud, Chinese cinnamon, angelica dahurica root, myrrh, frankincense, centella asiatica, saposhnikovia divaricata root, kaemferia galanga root, ginger,drynaria fortunei root, natural latex rubber

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackagepackagepackagepackagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1547758camphor 3.5 % / menthol 2.3 % / methyl salicylate 14.6 % Medicated PatchPSN4
1547758camphor 0.035 MG/MG / menthol 0.023 MG/MG / methyl salicylate 0.146 MG/MG Medicated PatchSCD4
1547758camphor 3.5 % / menthol 2.3 % / methyl salicylate 14.6 % Medicated PatchSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51367-021-08Shang Shi Zhi Tong Pain Relieving Plaster8 in 1 PACKAGEPLASTER84

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51367-021SHANG SHI ZHI TONG PAIN RELIEVING PLASTER (METHYL SALICYLATE, CAMPHOR, MENTHOL) PLASTER [INTERNATIONAL NATURE NUTRACEUTICALS]4Legacy NDC, 1 package rows20241222_f63f1b01-279b-4d76-b5f9-3feea2d05545.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
CENTELLA ASIATICAINACTIVE INGREDIENT7M867G6T1U1
CHINESE CINNAMONINACTIVE INGREDIENTWS4CQ062KM1
CLOVEINACTIVE INGREDIENTK48IKT53211
DRYNARIA FORTUNEI ROOTINACTIVE INGREDIENT731W842X8Q1
FRANKINCENSEINACTIVE INGREDIENTR9XLF1R1WM1
GINGERINACTIVE INGREDIENTC5529G5JPQ1
KAEMPFERIA GALANGA ROOTINACTIVE INGREDIENT7B7U9D12AI1
MYRRHINACTIVE INGREDIENTJC71GJ1F3L1
NATURAL LATEX RUBBERINACTIVE INGREDIENT2LQ0UUW8IN1
SAPOSHNIKOVIA DIVARICATA ROOTINACTIVE INGREDIENT8H84LFK2QD1
SCHIZONEPETA TENUIFOLIA FLOWERING TOPINACTIVE INGREDIENT2FN3BA1MZE1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51367-02151367-021-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYL SALICYLATELAV5U5022YACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB
CLOVEK48IKT5321IACT
NEPETA TENUIFOLIA FLOWERING TOP2FN3BA1MZEIACT
GINGERC5529G5JPQIACT
CHINESE CINNAMONWS4CQ062KMIACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
MYRRHJC71GJ1F3LIACT
FRANKINCENSER9XLF1R1WMIACT
CENTELLA ASIATICA7M867G6T1UIACT
SAPOSHNIKOVIA DIVARICATA ROOT8H84LFK2QDIACT
KAEMPFERIA GALANGA ROOT7B7U9D12AIIACT
DRYNARIA FORTUNEI ROOT731W842X8QIACT
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
GINGERGINGERC5529G5JPQSYRUP / ORAL0.05 ml/5mlExact identifier — unii candidate
2 equally ranked IID candidates
GINGERGINGERC5529G5JPQELIXIR / ORAL10 mg/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
c7090a37-fc54-4a03-9ebc-6ecca29cab02f63f1b01-279b-4d76-b5f9-3feea2d055452024-12-19WarningsExact identifier
spl id: c7090a37-fc54-4a03-9ebc-6ecca29cab02
spl set id: f63f1b01-279b-4d76-b5f9-3feea2d05545

Reported adverse events (FAERS/openFDA)#

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