The following Structured Product Label (SPL) was submitted to the FDA by Bioactive Nutritional, Inc. for the product Fng (NDC 43857-0424). 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 label display:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Echinacea (Angustifolia) 3X, Lomatium Dissectum 3X, Nasturtium Aquaticum 3X, Tabebuia Impetiginosa 3X, Hydrastis Canadensis 5X, Iodium 6X, Adrenalinum 8X, Argentum Metallicum 8X, Thymus (Suis) 8X, Thyroidinum (Suis) 8X, Phosphoricum Acidum 12X, Candida Albicans 12X, 30X, Lycopodium Clavatum 30X, Pulsatilla (Vulgaris) 30X, Sepia 30X.
For temporary relief of bloating of the stomach, flatulence, and allergic rhinitis.
For temporary relief of bloating of the stomach, flatulence, and allergic 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 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
FNG II
1 FL OZ (30 ml)
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