MedDataToolHigh Vitality
Generic: Agnus Castus, Ambra Grisea, Petroselinum Sativum, Estradiol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, Alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Gaba, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus Suis, Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Apiolum,
Estradiol Congeners✓ FDA-verified
View full FDA label ↗High Vitality is a homeopathic remedy designed to temporarily relieve symptoms like fatigue, joint pain, and muscle soreness. It works by using natural ingredients to help support your body’s healing processes. You take it by placing 1 to 10 drops under your tongue three times a day, or as directed by a healthcare professional. If you are pregnant or breastfeeding, it's important to consult a health professional before using it. Additionally, if you have children under 12, you should talk to a doctor before giving it to them.
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Uses
- fatigue. joint pain. muscle soreness.
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Dosage
Take 1-10 drops under the tongue, 3 times a day.
Consult a physician for use in children under 12 years of age.
Always follow your doctor's specific instructions for your dose.
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Side effects
Common
FatigueJoint painMuscle soreness
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Warnings
⚠ Important warnings
- If pregnant or breast-feeding, ask a health professional before use.
- Keep out of reach of children.
- In case of overdose, contact a physician or Poison Control Center right away.
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Answers pulled from the FDA label only.
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Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).