Viscumforce Liquid
FDA Label NDC 43857-0109

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bioactive Nutritional, Inc. for the product Viscumforce (NDC 43857-0109). 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:, indications:, warnings:, directions:, inactive ingredients:, keep out of reach of children:, questions:, package label display:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients:

Passiflora Incarnata 3X, Valeriana Officinalis 3X, Aurum Metallicum 12X, Baryta Carbonica 12X, Glonoinum 12X, Phosphorus 12X, Plumbum Metallicum 12X, Viscum Album 12X.

Indications:

For temporary relief of buzzing and stopped-up feeling in ears, cold feet, and numbness in the limbs.

For temporary relief of buzzing and stopped-up feeling in ears, cold feet, and numbness in the limbs.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Questions:

Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com

Package Label Display:

BIOActive Nutritional

VISCUMFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

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