Viscum Abietis Series 3 7ml
FDA Label NDC 48951-9265

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Viscum Abietis Series 3 7ml (NDC 48951-9265). 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 indications & usage, dosage & administration, otc - active ingredient, otc - purpose, inactive ingredient, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Indications & Usage

Directions: FOR ORAL USE.

Dosage & Administration

Take the contents of one ampule
under the tongue and hold for
30 seconds, then swallow.

Otc - Active Ingredient

Active Ingredient: Viscum Abietis (Fir tree mistletoe) 1 amp 1mg = 3X, 2 amps 5mg = 1 gm contains: 2X, 500mg,
3 amps 10mg = 2X,1 amp 20mg= 1 gm contains: 1X, 200mg

Otc - Purpose

Use: Temporary relief of headache.

Inactive Ingredient

Inactive Ingredients: Water, Salt

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Otc - Questions


Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

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