FDA.reportPublic FDA data

Shao Lin Pain Relief Plaster

Manufacturer
Zhejiang Dingtai Pharmaceutical Co.; Ltd
Effective date
2021-10-19
Label type
HUMAN OTC DRUG LABEL
Version
32747
Source
full-release
Hydrated at
2026-05-31 23:44:20

Label at a glance#

ProductShao Lin Pain Relief Plaster
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure16 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

Adults and children 12 years of age and older: Apply one or two plasters to affected area once a day. Remove after 12 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, consult a doctor. Refer to the above warnings: use otherwise than as directed may be dangerous.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol   0.5%

Methyl Salicylate  0.5%

Purpose

OTC - PURPOSE SECTION

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

Warning

WARNINGS SECTION

For External Use Only.

Do Not Use

OTC - DO NOT USE SECTION

on wounds

on irritated or damaged skin

if the appearance of this product has changed

in excess of 12 hours

if you have known hypersensitive to this product

otherwise than as directed

Ask a Doctor or Pharmacist Before Use If You Are

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant

taking other medications

When Using This Product

OTC - WHEN USING SECTION

avoid contact with the eye or mucous membranes

do not bandage tightly

supervise use by children

use caution if prone to allergic reactions

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

when using for pain of arthritis

pain persists for more than 10 days

redness is present

in conditions affecting children under 12 years of age

Keep Out of Reach of Children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If 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 12 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, consult a doctor.
Refer to the above warnings: use otherwise than as directed may be dangerous.

Other Information

OTHER SAFETY INFORMATION

Keep container tightly closed.

Store below 20 ℃ (68 ℉) in a dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

PEPPERS, LINDERA AGGREGATA ROOT, BLETILLA STRIATA BULB, ANGELICA DAHURICA ROOT, AMPELOPSIS JAPONICA ROOT, PAWPAW, SPARGANIUM STOLONIFERUM WHOLE, CURCUMA ZEDOARIA LEAF, ANGELICA SINENSIS ROOT, PAEONIA VEITCHII ROOT, CINNAMON, RHEUM PALMATUM WHOLE, FORSYTHIA SUSPENSA WHOLE, DRAGON'S BLOOD, FRANKINCENSE, MYRRH, PANAX NOTOGINSENG ROOT, ACACIA CATECHU WHOLE, BORNEOL

Questions or Comments?

OTC - QUESTIONS SECTION

Call (626)350-5000 or

E-mail: upc168@sbcglobal.net

Manufacturerd by

SPL UNCLASSIFIED SECTION

Zhejiang Dingtai Pharmaceutical Co.; Ltd

No. 1392, Huancheng South Road, Economy Development Zone,

Tongxiang, Zhejiang 314500, China

Distributed by

SPL UNCLASSIFIED SECTION

UPC Medical Supplies, Inc.

11030 Weaver Avenue

South El Monte, CA 91733  USA

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1650234menthol 5 % / methyl salicylate 5 % Medicated PatchPSN32747
1650234menthol 0.05 MG/MG / methyl salicylate 0.05 MG/MG Medicated PatchSCD32747
1650234menthol 5 % / methyl salicylate 5 % Medicated PatchSY32747

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69070-001-052024-01-30C16284748780-11030e365-3318-111a-e063-dadaa90a10e2Zhejiang Dingtai Pharmaceutical Co.; Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69070-001-05Shao Lin Pain Relief Plaster5 in 1 BOXPLASTER532747
69070-001-05Shao Lin Pain Relief Plaster1 g in 1 PATCHPLASTER132747

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69070-001SHAO LIN PAIN RELIEF PLASTER (MENTHOL, METHYL SALICYLATE) PLASTER [ZHEJIANG DINGTAI PHARMACEUTICAL CO.; LTD]32747Legacy NDC, 2 package rows20211020_f1139b34-4b52-4e72-8a55-02eb3dd8ce8c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3A3127
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y3127
MENTHOLACTIVE MOIETYL7T10EIP3A3127
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ3127
ACACIA CATECHU WHOLEINACTIVE INGREDIENTTJ6XA84OQF3127
AMPELOPSIS JAPONICA ROOTINACTIVE INGREDIENTO2672197TF3127
ANGELICA DAHURICA ROOTINACTIVE INGREDIENT1V63N2S9723127
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG3127
BLETILLA STRIATA BULBINACTIVE INGREDIENT00T5SH6SEJ3127
BORNEOLINACTIVE INGREDIENTM89NIB437X3127
CINNAMONINACTIVE INGREDIENT5S29HWU6QB3127
CURCUMA ZEDOARIA LEAFINACTIVE INGREDIENTM9E9LQH7N43127
DRAGON'S BLOODINACTIVE INGREDIENTM3YJ2C28IC3127
FORSYTHIA SUSPENSA WHOLEINACTIVE INGREDIENTRO2K2K561Z3127
FRANKINCENSEINACTIVE INGREDIENTR9XLF1R1WM3127
LINDERA AGGREGATA ROOTINACTIVE INGREDIENT517Q7XRT2T3127
MYRRHINACTIVE INGREDIENTJC71GJ1F3L3127
PAEONIA VEITCHII ROOTINACTIVE INGREDIENTVX6GD6M93V3127
PANAX NOTOGINSENG ROOTINACTIVE INGREDIENTGQX1C1175U3127
PAWPAWINACTIVE INGREDIENT8P95FP65YO3127
PEPPERSINACTIVE INGREDIENTT5KDM4J2393127
RHEUM PALMATUM WHOLEINACTIVE INGREDIENT75P857ARCY3127
SPARGANIUM STOLONIFERUM WHOLEINACTIVE INGREDIENT873IV8AW3C3127

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69070-00169070-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
PEPPERST5KDM4J239IACT
LINDERA AGGREGATA ROOT517Q7XRT2TIACT
BLETILLA STRIATA BULB00T5SH6SEJIACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
AMPELOPSIS JAPONICA ROOTO2672197TFIACT
PAWPAW8P95FP65YOIACT
SPARGANIUM STOLONIFERUM WHOLE873IV8AW3CIACT
CURCUMA ZEDOARIA LEAFM9E9LQH7N4IACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
PAEONIA VEITCHII ROOTVX6GD6M93VIACT
CINNAMON5S29HWU6QBIACT
RHEUM PALMATUM WHOLE75P857ARCYIACT
FORSYTHIA SUSPENSA WHOLERO2K2K561ZIACT
DRAGON'S BLOODM3YJ2C28ICIACT
FRANKINCENSER9XLF1R1WMIACT
MYRRHJC71GJ1F3LIACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
ACACIA CATECHU WHOLETJ6XA84OQFIACT
BORNEOLM89NIB437XIACT

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
CINNAMONCINNAMON5S29HWU6QBCAPSULE / ORALNAExact identifier — unii candidate
2 equally ranked IID candidates
CINNAMONCINNAMON5S29HWU6QBELIXIR / ORAL10.5 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
7716374a-a783-4389-8366-8d491224f94ef1139b34-4b52-4e72-8a55-02eb3dd8ce8c2021-10-19WarningsExact identifier
spl id: 7716374a-a783-4389-8366-8d491224f94e
spl set id: f1139b34-4b52-4e72-8a55-02eb3dd8ce8c

Reported adverse events (FAERS/openFDA)#

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