Viscum Salicis
FDA Label NDC 48951-1007

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 Salicis (NDC 48951-1007). 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 dosage & administration, otc - active ingredient, otc - purpose, inactive ingredient, indications & usage, otc - keep out of reach of children, warnings, otc - pregnancy or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Dosage & Administration

Directions: FOR ORAL USE ONLY. Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Otc - Active Ingredient

Active Ingredient: Viscum album (Salicis) 1 gm contains:
A13X 93.7%
B10X 37.5%
C7X 15.6%
D6X 31.2%
E5X 62.5%
F3X 12.5%
G2X 25%

Otc - Purpose

Inactive Ingredient

Inactive Ingredients: Water, Salt

Indications & Usage

Use: Temporary relief of headache.

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.

Otc - Pregnancy Or Breast Feeding

If you are pregnant or nursing, consult a doctor before use.

Otc - Do Not Use

Other

Natural ingredients may cause color, scent and/or taste variation.

Otc - Questions

Questions? Call 866 642-2858

Uriel, East Troy, WI 53120

www.urielpharmacy.com

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