The following Structured Product Label (SPL) was submitted to the FDA by Bioactive Nutritional, Inc. for the product Universaltox (NDC 43857-0534). 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:, keep out of reach of children:, directions:, inactive ingredients:, questions:, package display label:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Alfalfa 3X, Avena Sativa 3X, Fucus Vesiculosus 4X, Hordeum Vulgare 4X, Nasturtium Aquaticum 4X, Raphanus Sativus 4X, Triticum Aestivum 4X, Iodium 6X, Ubiquinone 6X, Glandula Suprarenalis Suis 8X, Hepar Suis 8X, Manganum Gluconate 8X, Oryza Sativa 8X, Thyroidinum (Suis) 8X, Calcarea Carbonica 12X, Natrum Muriaticum 12X, Pulsatilla (Pratensis) 12X, Rhus Tox 12X, Cortisone Aceticum 30X.
For temporary relief of sinus congestion, dry cough in the evening and rhinitis.
For temporary relief of sinus congestion, dry cough in the evening and rhinitis.
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 a cool, dry place.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.
Demineralized water, 25% Ethanol.
Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com
BIOActive Nutritional
UNIVERSALTOX
HOMEOPATHIC
1 FL OZ (30 ml)
Universaltox (Bani0027 Universaltox V02) 
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