FDA.reportPublic FDA data

Shennong Analgesic Plaster

Manufacturer
Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd | Guangdong Zhanjiang Jimin Pharmaceutical Co, Ltd | Guangdong Zhangjiang Jimin Pharmaceutical Co. Ltd
Effective date
2016-03-16
Label type
HUMAN OTC DRUG LABEL
Version
3189
Source
full-release
Hydrated at
2026-05-31 22:46:10

Label at a glance#

ProductShennong Analgesic Plaster
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure12 sections

Indications and uses

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

Dosage and administration

Clean and dry the affected area. Remove the paper backing from the plaster. Apply the plaster to the affected area. Change plasters as needed, but do not apply more than 3 to 4 times daily. Children under 12 years of age: contact a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor    4.28%

Menthol      2.84%

Methyl Salicylate  1.4%

Purpose

OTC - PURPOSE SECTION

Camphor                  External Analgesic

Menthol                    External Analgesic

Methyl Salicylate       External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints due to:

Simple backache, arthritis, strains, bruises, sprains.

Warnings

WARNINGS SECTION

For external use only.

Do not use on pregnant woman.

Do not use

OTC - DO NOT USE SECTION

on wounds, irritated or damaged skin, otherwise than as directed.

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes or mucous membranes.

Do not bandage tightly.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens.

Symptoms persist for more than 7 days.

Symptoms clear up and occur again within a few days.

Excessive irritation of the skin develops.

Nausea, vomiting, abdominal discomfort, diarrhea or skin rash occurs.

When using for pain of arthritis: pain persists for more than 10 days and if redness is present.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean and dry the affected area. Remove the paper backing from the plaster. Apply the plaster to the affected area. Change plasters as needed, but do not apply more than 3 to 4 times daily.

Children under 12 years of age: contact a doctor.

Other Information

OTHER SAFETY INFORMATION

Keep tightly closed.

Store at room temperature, 20 to 25 °C (68-77 °F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

PANAX PSEUDOGINSENG ROOT, ANGELICA DAHURICA ROOT, CIBOTIUM BAROMETZ ROOT, NOTOPTERYGIUM INCISUM ROOT, SAPOSHNIKOVIA DIVARICATA ROOT, ACTAEA CIMICIFUGA ROOT, SAFFLOWER, LIGUSTICUM WALLICHII ROOT, ANGELICA SINENSIS ROOT, MYRRH, PARIS POLYPHYLLA WHOLE, FRANKINCENSE, BASIL OIL, ATROPA BELLADONNA, NATURAL LATEX RUBBER, ROSIN, ZINC OXIDE, PETROLATUM, LANOLIN

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1793754camphor 4.28 % / menthol 2.84 % / methyl salicylate 1.4 % Medicated PatchPSN3189
1793754camphor 0.0428 MG/MG / menthol 0.0284 MG/MG / methyl salicylate 0.014 MG/MG Medicated PatchSCD3189
1793754camphor 4.28 % / menthol 2.84 % / methyl salicylate 1.4 % Medicated PatchSY3189

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68048-922-082020-01-31C16284748780-19d75b9d0-5e9c-f424-e053-dadaa90a57ceGuangdong Zhanjiang Jimin Pharmaceutical Co, Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68048-922-08Shennong Analgesic Plaster2.5 mg in 1 PATCHPLASTER2.53189
68048-922-08Shennong Analgesic Plaster8 in 1 BOXPLASTER83189

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68048-922SHENNONG ANALGESIC PLASTER (CAMPHOR, MENTHOL, METHYL SALICYLATE) PLASTER [GUANGDONG ZHANJIANG JIMIN PHARMACEUTICAL CO. LTD]3189Legacy NDC, 2 package rows20160601_f635bfa5-6b55-48a4-9de8-c569df60a294.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68048-92268048-922-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
PANAX PSEUDOGINSENG ROOTNMK0ZS613UIACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
CIBOTIUM BAROMETZ ROOT2YP9JGT10RIACT
NOTOPTERYGIUM INCISUM ROOT5Z2WW4J6RIIACT
SAPOSHNIKOVIA DIVARICATA ROOT8H84LFK2QDIACT
ACTAEA CIMICIFUGA ROOT65J267BAZTIACT
SAFFLOWER4VBL71TY4YIACT
LIGUSTICUM WALLICHII ROOTR81AD159QSIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
MYRRHJC71GJ1F3LIACT
PARIS POLYPHYLLA WHOLE1E5W175DRXIACT
FRANKINCENSER9XLF1R1WMIACT
BASIL OILZ129UMU8LEIACT
ATROPA BELLADONNAWQZ3G9PF0HIACT
NATURAL LATEX RUBBER2LQ0UUW8INIACT
ROSIN88S87KL877IACT
ZINC OXIDESOI2LOH54ZIACT
PETROLATUM4T6H12BN9UIACT
LANOLIN7EV65EAW6HIACT

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
6a4b574a-93bb-425c-87a3-8638c72f7bcbf635bfa5-6b55-48a4-9de8-c569df60a2942016-03-16WarningsExact identifier
spl id: 6a4b574a-93bb-425c-87a3-8638c72f7bcb
spl set id: f635bfa5-6b55-48a4-9de8-c569df60a294

Reported adverse events (FAERS/openFDA)#

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