Active Ingredients:
Colchicum Autumnale 30X, Lacticum Acidum 30X, Lycopodium Clavatum 30X, Phosphoricum Acidum 30X, Phosphorus 30X, Syzygium Jambolanum 30X, Uranium Nitricum 30C.
Glucoseforce Liquid
FDA Label NDC 43857-0648
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 Glucoseforce (NDC 43857-0648). 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:, purpose:, warnings:, keep out of reach of children:, directions:, indications:, inactive ingredients:, questions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
For temporary relief of symptoms due to abnormal blood sugar.
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.
Keep Out Of Reach Of Children:
In case of overdose, get medical help or contact a Poison Control Center right away.
Directions:
10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.
Indications:
For temporary relief of symptoms due to abnormal blood sugar.
Inactive Ingredients:
Demineralized Water, 25% Ethanol
Questions:
Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com
Package Label Display:
BIOActiveNutritional
GLUCOSEFORCE-HP
HOMEOPATHIC
1 FL OZ (30 ml)
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