Mytox Spray
Product Images NDC 83027-0092

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Mytox (Nspc0101 Mytox)

Mytox (Nspc0101 Mytox)
This is a description for a homeopathic product called "MYTOX". It is indicated for temporary relief of symptoms associated with fungal conditions, such as night sweats, headache, fatigue, muscle aches, joint pain, and itchy, red or scaly skin. The product is for professional use only and should not be used by pregnant or breastfeeding individuals without consulting a health professional. In case of overdose, medical help or contact with a Poison Control Center should be sought immediately. The product should be kept out of reach of children and should not be used if the tamper-evident seal is broken or missing. The product is to be stored in a cool place after opening. The claims of the product are based on traditional homeopathic practice and have not been evaluated by the FDA. The product contains active ingredients such as Borax, Colchicum Autumnale, Drosera (Rotundifolia), Arsenicum Album, Ubidecarenonum (CoQ 10), Agaricus Muscarius, and Bufo Rana. It also contains inactive ingredients like Alcohol USP and Purified Water USP. The recommended dosage for adults is 2 to 3 sprays orally, three times daily, while children under twelve should take half the adult dosage. It is advised not to take the product within 15 minutes of consuming food, beverage, or brushing teeth, and a physician should be consulted for use in children under 12 years of age. The product is manufactured exclusively for Nutritional Specialties, Inc., and can be contacted at PO Box 97227, Pittsburgh, PA 15229.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.