Plaster

Manufacturer
Dah Wei Chem & Pharm Co., Ltd.
Effective date
2011-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:29:35

Label at a glance#

ProductPlaster MandAHerbalPlaster
Active ingredientMENTHOL, METHYL SALICYLATE, CAMPHOR (SYNTHETIC), MYRRH, SESAME OIL
Label structure10 sections

Storage and handling

■ Keep container tightly closed, once opened, fold the opening and keep pressed closed with a clip. ■ Store at room temperature.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: (each 5 g patch contains)                                 PURPOSE
METHYL SALICYLATE  250 mg                                         EXTERNAL ANALGESIC
L-METHENOL -  200 mg                                                    EXTERNAL ANALGESIC
CAMPHOR –   40mg                                                         EXTERNAL ANALGESIC
SESAME OIL – 500 mg                                                     EXTERNAL ANALGESIC
MYRRH – 150mg                                                              EXTERNAL ANALGESIC                                     
                                  

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis strains, bruises and sprains.

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

Remove the clear backing and apply to thew sore area of skin.

STORAGE AND HANDLING SECTION

■ Keep container tightly closed, once opened, fold the opening and keep pressed closed with a clip.
■ Store at room temperature.

INACTIVE INGREDIENT SECTION

Inactive ingredient: Resin

OTC - ASK DOCTOR SECTION


Stop use and ask a doctor if:
■ Condition worsens
■ Symptom clear up and occur again within a few days.
■ Symptom persist for more than 7 days.
■ Nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
■ Excessive irritation of the skin develops
■ When using for pain of arthritis:
■ In conditions affecting children under 12 years of age
■ If red nose is present
■ If pain persists for more than 10 days 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out reach of children to avoid accidental poisoning. If swallowed, get medical help or consult a poison control center right away.

OTC - DO NOT USE SECTION

Do not use:
■ On wounds
■ On infected or damaged skin
When using this product:
■ Avoid contact with eyes or mucous membranes.
■ Do not bandage tightly.

PURPOSE

OTC - PURPOSE SECTION

EXTERNAL ANALGESIC

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MandAHerbalPlasterMandAHerbalPlaster

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
14319-3118-52019-10-29C16284748780-1960f7f55-cb4b-8e05-e053-dbdaa90a074aMandAHerbalPlaster

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14319-3118-5PlasterMandAHerbalPlaster6 in 1 POUCHPATCH61
14319-3118-5PlasterMandAHerbalPlaster30 g in 1 PATCHPATCH301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14319-3118PLASTER MANDAHERBALPLASTER (MENTHOL) PATCH [DAH WEI CHEM & PHARM CO., LTD.]1Legacy NDC, 2 package rows20110916_c2207dbf-4b12-4742-bc29-8f7ec317475a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET1
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
MYRRHACTIVE INGREDIENTJC71GJ1F3L1
SESAME OILACTIVE INGREDIENTQX10HYY4QV1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET1
MENTHOLACTIVE MOIETYL7T10EIP3A1
METHYL SALICYLATEACTIVE MOIETYLAV5U5022Y1
MYRRHACTIVE MOIETYJC71GJ1F3L1
SESAME OILACTIVE MOIETYQX10HYY4QV1
PINUS TABULIFORMIS BARKINACTIVE INGREDIENT3G75L8C3RU1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14319-311814319-3118-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
a4f660cb-f504-4f9c-9c3b-5cb4faf0d07ac2207dbf-4b12-4742-bc29-8f7ec317475a2011-06-08WarningsExact identifier
spl id: a4f660cb-f504-4f9c-9c3b-5cb4faf0d07a
spl set id: c2207dbf-4b12-4742-bc29-8f7ec317475a

Reported adverse events (FAERS/openFDA)#

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