Active Ingredients:
Lappa Major 3X, Trifolium Pratense 3X, Phytolacca Decandra 4X, Hydrocotyle Asiatica 6X, Arsenicum Album 12X, Graphites 12X, Mezereum 12X.
Epiforce E Liquid
FDA Label NDC 43857-0570
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 Epiforce E (NDC 43857-0570). 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 skin irritations, urticaria and eczema.
For temporary relief of skin irritations, urticaria and eczema.
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 Label Display:
BIOActive Nutritional
EPIFORCE E
HOMEOPATHIC
1 FL OZ (30 ml)
* Please review the disclaimer below.
