Arnica Montana 3x, 6x, 12x, 30x, 200x Tablet
FDA Label NDC 62795-1112

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 Arnica Montana 3x, 6x, 12x, 30x, 200x (NDC 62795-1112). 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. hendelarnica montana 3x, 6x, 12x, 30x, 200x, 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 Hendel Arnica montana 3X, 6X, 12X, 30X, 200X 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

• Symptoms of bruising

• Pain

Active Ingredient

Arnica Montana 3X, 6X, 12X, 30X, 200X

Inactive Ingredient

Lactose, Magnesium stearate

Directions

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.

Uses

For the temporary relief of:

• Symptoms of bruising

• Pain

* Please review the disclaimer below.