WU YANG BRAND MEDICATED

Manufacturer
GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY
Effective date
2019-11-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:33

Label at a glance#

ProductWU YANG BRAND MEDICATED
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure12 sections

Storage and handling

Other information keep in a tightly closed container store at room temperature 15º to 30º C (59º to 86º F), away from sunlight

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Menthol 6%
Methyl salicylate 10%

OTC - PURPOSE SECTION

Purpose
External analgesic
External analgesic

INDICATIONS & USAGE SECTION

Uses
For the temporary relief of minor aches and pains of muscles and joints due to:
simple backache
arthritis
strains
bruises
sprains

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use
on wounds
on damaged or irritated skin
if excessive irritation develops
otherwise than as directed. To do so may be dangerous.

OTC - WHEN USING SECTION

When using this product
avoid contact with the eyes or mucous membranes
do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if
condition worsens
symptoms persist for more than 7 days
symptoms clear up and occur again within a few days
when using for pain of arthritis:
if pain persists for more than 10 days
if redness is present
in conditions affecting children under 12 years of age

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.

DOSAGE & ADMINISTRATION SECTION

Directions
Adults and children 2 years of age and older: Cut to desired size, remove clear backing, and apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Do not use, consult a doctor.

STORAGE AND HANDLING SECTION

Other information
keep in a tightly closed container
store at room temperature 15º to 30º C (59º to 86º F), away from sunlight

OTC - QUESTIONS SECTION

Questions or comments? (888) 221-3496 M-F 9 am to 5 pm
you may also report serious side effects to this phone number

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WU YANG BRAND MEDICATED PLASTER

NDC 61822-0045-1

External Analgesic

10 Plasters – 3.9 x 11 inches (10 x 28 cm) each

Box2Box2

WU YANG BRAND MEDICATED PLASTER

NDC 61822-0045-2

External Analgesic

1 Plaster – 3.9 x 78.7 inches (10 x 200 cm)

Box1Box1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1541608menthol 6 % / methyl salicylate 10 % Medicated PatchPSN2
1541608menthol 0.06 MG/MG / methyl salicylate 0.1 MG/MG Medicated PatchSCD2
1541608menthol 6 % / methyl salicylate 10 % Medicated PatchSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61822-0045-12021-01-29C16284748780-1ba0f9c33-5d27-a910-e053-dadaa90a0b85Drug Facts
61822-0045-22021-01-29C16284748780-1ba0f9c33-5d27-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61822-0045-1WU YANG BRAND MEDICATED10 in 1 BOXPLASTER102
61822-0045-2WU YANG BRAND MEDICATED1 in 1 CANPLASTER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61822-0045WU YANG BRAND MEDICATED (MENTHOL, METHYL SALICYLATE) PLASTER [GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY]2Legacy NDC, 2 package rows20191119_b4ee1d1b-0eed-4ae7-ad78-666b0fd15213.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
MENTHOLACTIVE MOIETYL7T10EIP3A1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
BLACK CATECHUINACTIVE INGREDIENT55J167EEON1
DAEMONOROPS DRACO RESININACTIVE INGREDIENT787Z7N9UCU1
DIPSACUS ASPER ROOTINACTIVE INGREDIENTLB1GQP42531
DRYNARIA FORTUNEI ROOTINACTIVE INGREDIENT731W842X8Q1
GARDENIA JASMINOIDES FRUITINACTIVE INGREDIENT7CTH8MD5491
LONICERA JAPONICA FLOWERINACTIVE INGREDIENT4465L2WS4Y1
MAMMAL BONE, FOSSILIZEDINACTIVE INGREDIENT0N1T3913DA1
MYRRHINACTIVE INGREDIENTJC71GJ1F3L1
POLYGONUM CUSPIDATUM WHOLEINACTIVE INGREDIENT1VDG5Y5HS61
SAFFLOWERINACTIVE INGREDIENT4VBL71TY4Y1
TARAXACUM MONGOLICUMINACTIVE INGREDIENT4E8QL88U6H1

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61822-004561822-0045-1, 61822-0045-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
9f62ec35-246b-4b13-9b21-18e5cddb5cb8b4ee1d1b-0eed-4ae7-ad78-666b0fd152132019-11-13WarningsExact identifier
spl id: 9f62ec35-246b-4b13-9b21-18e5cddb5cb8
spl set id: b4ee1d1b-0eed-4ae7-ad78-666b0fd15213

Reported adverse events (FAERS/openFDA)#

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