Active Ingredients:
Apis Mellifica 12X, Cantharis 12X, Graphites 12X, Natrum Muriaticum 12X, Rhus Glabra 12X, Rhus Toxidodendron 12X, Rhus Venenata 12X, Urtica Dioica 12X
Rhustoxoforce Liquid
FDA Label NDC 43857-0206
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 Rhustoxoforce (NDC 43857-0206). 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:
For temporary relief of allergies caused by poison ivy, oak, and summac.
For temporary relief of allergies caused by poison ivy, oak, and summac.
Warnings:
If pregnant or breast-feeding, ask a health care professional befure 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:
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
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:
BioActie Homeopathic
RHUSTOXOFORCE
1 FL OZ (30 mL)
* Please review the disclaimer below.
