Active Ingredients:
Calcarea Carbonica 30X, Calcarea Fluorica 30X, Calcarea Phosphorica 30X, Hekla Lava 30X, Hydrofluoricum Acidum 30X, Rhus Tox 30X, Silicea 30X, Symphytum Officinale 30X.
Boneforce Liquid
FDA Label NDC 43857-0591
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 Boneforce (NDC 43857-0591). 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.
Label Section Quick Index
Indications:
For temporary relief of injuries to bones, tendons, and muscles.
For temporary relief of injuries to bones, tendons, and muscles.
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.
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.
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
Questions:
Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com
Package Label Display:
BIOActive Nutritional
BONEFORCE-HP
HOMEOPATHIC
1 FL OZ (30 ml)
* Please review the disclaimer below.
