Emvita 28
Cerebrum, Helleborus niger, Hyoscyamus niger, Mandragora · Liquid · Oral
Active ingredient
Drug Facts Active Ingredients: (HPUS*) 25% of each Cerebrum 21X Helleborus niger 18LM Hyoscyamus niger 21X Mandragora 800C *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: Judgemental Behavior
Uses
Uses: (†) Homeopathic remedy for general well being: judgemental behavior.
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
- Sus Scrofa Cerebrum in 1 product
- Helleborus Niger Root in 1 product
- Sus Scrofa Pituitary Gland in 1 product
- Mandragora Officinarum Root in 1 product
Emvita 28 NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 66343-115 | Sus Scrofa Cerebrum 21 [hp_X]/60mL; Helleborus Niger Root 18 [hp_M]/60mL; Sus Scrofa Pituitary Gland 21 [hp_X]/60mL;… Liquid | RUBIMED AG | UNAPPROVED HOMEOPATHIC |
Frequently asked questions
What is Emvita 28 used for?
Uses: (†) Homeopathic remedy for general well being: judgemental behavior.
Who makes Emvita 28?
Emvita 28 is listed by 1 labeler in the FDA NDC directory, including RUBIMED AG.