Active Ingredients:
Antimonium Crudum 12X, Belladonna 12X, Calcarea Carbonica 12X, Calcarea Fluorica 12X, Calcarea Phosphorica 12X, Hekla Lava 12X, Mercurius Solubilis 12X, Plumbum Metallicum 12X, Sepia 12X, Silicea 12X, Hydrofluoricum Acidum 30X.
Dentaforce Liquid
FDA Label NDC 43857-0093
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 Dentaforce (NDC 43857-0093). 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.
Label Section Quick Index
Indications:
For temporary relief of gum, dentition, and tooth pain.
For temporary relief of gum, dentition, and tooth pain.
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:
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 Display Label:
BioActive Homeopathic
DENTAFORCE
1 FL OZ (30 mL)
* Please review the disclaimer below.
