The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product Dr. Hendel Arthritis Pain Relief (NDC 62795-1113). 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 warnings, keep out of reach of children, indications, active ingredient, inactive ingredient, directions, uses, dr. hendel arthritis pain relief, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or
worsen, a health professional should be consulted. Do not use if sensitivity to Hendel Arthritis Pain Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.
KEEP OUT OF REACH OF CHILDREN
Arthritis Pain Relief
Each tablet containsequal parts of: Bryonia 4X; Arnica montana 6X; Colchicum autumnale 6X; Dulcamara 6X; Harpagophytum 6X; Ledum palustre 6X; Rhododendron chrysanthum 6X; Symphytum officinale 6X; Rhus tox 8X, 12X, 30X; Calcarea carbonica 12X, Calcarea phosphorica 12X; Silicea 12X
Lactose, Magnesium stearate
Dosage: Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.
For the temporary relief of:
• Bone & joint pain
• Aching muscles
* Please review the disclaimer below.
