Arthosan

Manufacturer
Warsan Homoeopathic
Effective date
2018-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:14

Label at a glance#

ProductArthosan
Active ingredientHYPERICUM PERFORATUM, PSEUDOGNAPHALIUM OBTUSIFOLIUM, TOXICODENDRON PUBESCENS LEAF, COMFREY ROOT, COLCHICUM AUTUMNALE BULB, BERBERIS VULGARIS ROOT BARK, SOLANUM DULCAMARA TOP, GELSEMIUM SEMPERVIRENS ROOT, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, GINGER
Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

If pregnant or breast-feeding, ask health professional before use.

Do not use if tamper evident seal is missing or broken.

OTC - ACTIVE INGREDIENT SECTION

Berberis Vulgaris 1X
Bryonia Alba 1X
Colchicum 1X
Colocynthis 1X
Dulcamara 1X
Gelsemium Sempervirens 1X
Gnaphalium Polycephalum 1X
Hypericum Perforatum 1X
Rhus Toxicodendron 1X
Symphytum Officinale 1X
Zingiber 1X

OTC - PURPOSE SECTION

Temporary relief from minor muscle and joint aches and pains including: low back pain, leg pain, joint pain, bruises, arthritis, stiffness.

INACTIVE INGREDIENT SECTION

Purified Water

Alcohol

DOSAGE & ADMINISTRATION SECTION

Adults and children 18 years and older: One tablespoon three times daily.

Children and adolescents under the age of 18: Consult doctor prior to use.

INDICATIONS & USAGE SECTION

Temporary relief from minor muscle and joint aches and pains including: low back pain, leg pain, joint pain, bruises, arthritis, stiffness.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

arthosan feb 2018.jpgarthosan feb 2018.jpg

WARNINGS AND PRECAUTIONS SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69008-1001-92020-01-31C16284748780-19d75b9d0-9514-f424-e053-dadaa90a57ce6593de91-905d-e547-e053-2991aa0ad131

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69008-1001-9Arthosan240 mL in 1 BOTTLESOLUTION/ DROPS2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69008-1001ARTHOSAN (BERBERIS VULGARIS, BRYONIA ALBA, COLCHICUM, COLOCYNTHIS, DULCAMARA, GELSEMIUM SEMPERVIRENS) SOLUTION/ DROPS [WARSAN HOMOEOPATHIC]1Legacy NDC, 1 package rows20180219_6593de91-905d-e547-e053-2991aa0ad131.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69008-100169008-1001-9

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
6593de91-905e-e547-e053-2991aa0ad1316593de91-905d-e547-e053-2991aa0ad1312018-02-19WarningsExact identifier
spl id: 6593de91-905e-e547-e053-2991aa0ad131
spl set id: 6593de91-905d-e547-e053-2991aa0ad131

Reported adverse events (FAERS/openFDA)#

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