Hendel Rhus Tox Tablet
FDA Label NDC 62795-1127

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product Hendel Rhus Tox (NDC 62795-1127). 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, uses, keep out of reach of children, directions, indications, inactive ingredient, ingredients, hendel rhus tox, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warnings

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 Rhus Tox 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

Uses

For the temporary relief of:
• Painful Joints
• Muscle Aches
• Stiffness in Joints

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Directions

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

Indications

Painful Joints, Muscle Aches, Stiffness in Joints

Inactive Ingredient

Lactose, Magnesium stearate

Ingredients

Each tablet contains equal parts of Rhus Tox 6X, 12X, 30X, 200X.

* Please review the disclaimer below.