Hendel Fibromyalgia Symptom Relief
FDA Label NDC 62795-1117

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 Fibromyalgia Symptom Relief (NDC 62795-1117). 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, ingredients, inactive ingredient, directions, uses, 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 Fibromyalgia Symptom Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

Fibromyalgia Symptom Relief

Ingredients

Each tablet contains equal parts of Valeriana officinalis 2X; Arnica montana,radix 3X, 6X; Aconitum napellus 4X; Bryonia4X; Rhus tox 4X, 8X, 12X, 30X; Berberis vulgaris 6X; Colchicum autumnale 6X; Dulcamara6X, Harpagophytum 6X; Ledum palustre 6X; Rhododendron chrysanthum 6X

Inactive Ingredient

Lactose, Magnesium stearate

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

Uses

For the temporary relief of:

• Fatigue
• Muscle Pain
• Sleeplessness

* Please review the disclaimer below.