Active Ingredients:
Thymus (Suis) 8X.
Thymus Liquid
FDA Label NDC 43857-0194
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 Nutrional, Inc. for the product Thymus (NDC 43857-0194). 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.
Label Section Quick Index
Indications:
Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza.
Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza.
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 a cool, dry place.
Directions:
Three sprays per day. Hold in mouth for three minutes.
Inactive Ingredients:
Citric Acid, Demineralized Water, Glycerin, Sodium Benzoate.
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
Melbourne, FL 32935
For Nutritional Information write:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
Package Label Display:
BIOActive Nutritional
THYMUS
HOMEOPATHIC
1 FL OZ (30 ml)
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