Arthosan
FDA Label NDC 69008-1001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Warsan Homoeopathic for the product Arthosan (NDC 69008-1001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - keep out of reach of children, warnings, otc - active ingredient, otc - purpose, inactive ingredient, dosage & administration, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

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

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

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

* Please review the disclaimer below.