Emvita 7
Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus · Liquid · Oral
Active ingredient
Drug Facts Active Ingredients: (HPUS*) 20% of each Anacard occ 18LM Glandula sup 21X Lachesis mutus 800C Lycopodium 16LM Phosphorus 21X *The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Purpose
Homeopathic Medicine For General Well-being: Defiance
Uses
Uses: (†) Homeopathic remedy for general well being: defiance.
Warnings
Warnings: Stop use if symptoms persist or worsen. If you are pregnant or breastfeeding, consult a healthcare professional prior to use. Keep out of reach of children.
Keep out of reach of children
Keep out of reach of children.
Directions
Directions: (adults & children 6 years & older) Take 12 drops 2 times daily, or as recommended by your health care professional.
Inactive ingredients
Inactive ingredients: Ethanol 20% USP, Purified Water.
Questions?
Manufactured by: OHM pharma, Inc, USA. Distributed by: Privia Naturals, LLC. 9169 W State St #196 Garden City, ID 83714 www.privianaturals.com Info@privianaturals.com Product of USA.
Label text from the FDA structured product label by RUBIMED AG (revised Oct 29, 2024). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Anacardium Occidentale Fruit in 1 product
- Sus Scrofa Adrenal Gland in 1 product
- Lachesis Muta Venom in 1 product
- Lycopodium Clavatum Spore in 1 product
- Phosphorus in 1 product
Emvita 7 NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 66343-094 | Anacardium Occidentale Fruit 18 [hp_M]/60mL; Sus Scrofa Adrenal Gland 21 [hp_X]/60mL; Lachesis Muta Venom 800… Liquid | RUBIMED AG | UNAPPROVED HOMEOPATHIC |
Frequently asked questions
What is Emvita 7 used for?
Uses: (†) Homeopathic remedy for general well being: defiance.
Who makes Emvita 7?
Emvita 7 is listed by 1 labeler in the FDA NDC directory, including RUBIMED AG.