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WU YANG BRAND MEDICATED

Dosage form: plaster
Ingredients: MENTHOL 6g, METHYL SALICYLATE 10g
Labeler: GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY
NDC code: 61822-0045

Medically reviewed by Drugs.com. Last updated on Nov 4, 2024.

Drug Facts

Active ingredients
Menthol 6%
Methyl salicylate 10%

Purpose
External analgesic
External analgesic

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

Warnings
For external use only

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

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

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

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

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.

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

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

WU YANG BRAND MEDICATED PLASTER

NDC 61822-0045-1

External Analgesic

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

WU YANG BRAND MEDICATED PLASTER

NDC 61822-0045-2

External Analgesic

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

WU YANG BRAND MEDICATED 
menthol, methyl salicylate plaster
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61822-0045
Route of AdministrationTOPICAL, TRANSDERMALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL6 g
METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE10 g
Inactive Ingredients
Ingredient NameStrength
BLACK CATECHU 
POLYGONUM CUSPIDATUM WHOLE 
TARAXACUM MONGOLICUM 
DAEMONOROPS DRACO RESIN 
DRYNARIA FORTUNEI ROOT 
MAMMAL BONE, FOSSILIZED 
GARDENIA JASMINOIDES FRUIT 
LONICERA JAPONICA FLOWER 
SAFFLOWER 
DIPSACUS ASPER ROOT 
MYRRH 
Packaging
#Item CodePackage Description
1NDC:61822-0045-110 PLASTER in 1 BOX
2NDC:61822-0045-21 PLASTER in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/19/2001
Labeler - GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY (530854970)
Establishment
NameAddressID/FEIOperations
GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY530854970manufacture(61822-0045)

Revised: 11/2019
 
GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.