Hahnemann Headache
FDA Label NDC 63545-637

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hahnemann Laboratories, Inc. Dba Alpine Pharmaceuticals for the product Hahnemann Headache (NDC 63545-637). 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 active ingredients, purpose, keep out of reach of children, use, warnings, directions, inactive ingredient, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

ACTIVE INGREDIENT listed above

YTTRIUM IODATUM

Purpose

HEADACHE

Keep Out Of Reach Of Children

Keep out of reach of children.

Use

USE according to standard Homeopathic indications for self-limiting conditions, such as listed above. HEADACHE

Warnings

Warning: If pregnant, or nursing, or if symptoms persist consult your practitioner.

Directions

DIRECTIONS: Dissolve one dose under tongue. Repeat as needed or as directed. Stop taking if symptoms worsen.

DOSE: Adults and children take 10 - 15 pellets once or as directed by your prescriber.

Inactive Ingredient

INACTIVE INGREDIENTS: sucrose, lascose.

Package Label

YTTRIUM IODATUM    200C    HEADACHE   EST. 63545   Contains 5 g

HOMEOPATHIC MEDICINE

Hahnemann Laboratories Inc.   1940 Fourth St.  San Rafael, CA 94901

TWIST TO OPEN-USE ONLY IF SEALED

Questions: Toll free 888-427-6422

Hahnemann Headache1 (Hanmemann Headache1)

Hahnemann Headache1 (Hanmemann Headache1)

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