Hendel Nerve Pain Relief
FDA Label NDC 62795-1132

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 Nerve Pain Relief (NDC 62795-1132). 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, purpose, ingredients, inactive ingredient, directions, uses, hendel nerve pain relief, 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 Nerve 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

KEEP OUT OF REACH OF CHILDREN

Purpose

Nerve Pain Relief

Ingredients

Each tablet contains equal parts of Mezereum 3X; Arnica montana 6X; Arsenicum album 12X; Belladonna 6X; Colocynthis 6X; Gnaphalium polycephalum 6X; Hypericum perforatum 6X; Ruta graveolens 6X; Rhux tox 12X

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. If symptoms persist, take 1 tablet every hour; not to exceed 12 tablets daily.

Uses

For the temporary relief of:
• Tingling sensation
• Shooting pain

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