Mytox
Mytox is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Mytox 6021. Available dosage form: liquid.
Drug Details
- Generic Name
- Mytox
- Brand Names
- Mytox 6021
- Application Number
- Sponsor
- Professional Complementary Health Formulas
- NDC Codes
- 1
- Dosage Forms
- LIQUID
- Routes
- ORAL
- Active Ingredients
- SODIUM BORATE, COLCHICUM AUTUMNALE BULB, AMANITA MUSCARIA FRUITING BODY, ARSENIC TRIOXIDE, DROSERA ROTUNDIFOLIA WHOLE, BUFO BUFO CUTANEOUS GLAND, UBIDECARENONE
Indications and Usage
INDICATIONS For the temporary relief of red or itchy skin, cough, joint or muscle pain or stiffness, shortness of breath, sneezing, occasional headache, dizziness, or fatigue.*
Warnings
WARNINGS Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.