FDA.reportPublic FDA data

ArthriMed-Plus Spray 30 ml

Manufacturer
Multi Service
Effective date
2022-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:57:28

Label at a glance#

ProductArhtri Plus
Active ingredientMENTHOL, EUCALYPTUS OIL, CLOVE OIL
Label structure9 sections

Indications and uses

For the temporary relief of aches and pains of muscles and joints associated with backache, lumbago,strains, bruises,sprains and arthritic or rheumatic pain, pain of tendons and ligaments.

Dosage and administration

For adults and children 2 years of age and older: Shake well before use. Apply to the affected area not more than 3-4 times daily. Allow absorption to occur naturally for maximum penetration. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a health care practitioner.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.5%

Encalyptus oil (Eucalyptus globutus) (leaf) 3%

Clove Oil (Eugenia caryophyllatus) (leaf) 0.2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic


Uses

INDICATIONS & USAGE SECTION

For the temporary relief of aches and pains of muscles and joints associated with backache, lumbago,strains, bruises,sprains and arthritic or rheumatic pain, pain of tendons and ligaments.


Warnings

WARNINGS SECTION

For external use only. Do not apply to wounds or damaged skin. Do not inhale. Avoid contact with eyes and mucous membranes. Discontinue use if rash or irritation occurs. The application of external heat, such as an electric heating pad, may result in excessive skin irritation or skin burn. Do not bandage. Keep away from heat, sparks and open flames.


Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children 2 years of age and older: Shake well before use. Apply to the affected area not more than 3-4 times daily. Allow absorption to occur naturally for maximum penetration. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a health care practitioner.


Inactive Ingredients

INACTIVE INGREDIENT SECTION

Camphor, Lemongrass, Isopropyl Alcohol, Peppermint Oil, Purified Water

Other Information

SPL UNCLASSIFIED SECTION

Do not use if seal is broken.


Questions or comments?

OTC - QUESTIONS SECTION

info@multiservice.work

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Made in Canada

ArthriMed-Plus

Spray

Net Wt. 30 ml

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82760-00282760-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
ISOPROPYL ALCOHOLND2M416302IACT
PEPPERMINT OILAV092KU4JHIACT
WATER059QF0KO0RIACT
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
MENTHOLL7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
CLOVE OIL578389D6D0ACTIB

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
e5315d88-d40a-2023-e053-2995a90a194ce31bd69f-97ac-9d99-e053-2995a90a580e2022-08-01WarningsExact identifier
spl set id: e31bd69f-97ac-9d99-e053-2995a90a580e

Reported adverse events (FAERS/openFDA)#

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