Drugplain

Emvita 7 18 [hp_M]/60mL

Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus · LIQUID · RUBIMED AG

No Recall History
Plain English

Emvita 7 is a liquid containing anacard occ, glandula sup, lachesis mutus, lycopodium, phosphorus at 18 [hp_M]/60mL, taken oral. Manufactured by RUBIMED AG.

Key Facts

Brand Name
Emvita 7
Generic Name
Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus
NDC Code (Product)
66343-094
Manufacturer
RUBIMED AG
Strength
18 [hp_M]/60mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Marketing Start
12/21/2022

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective1 reports
exposure during pregnancy1 reports
increased bronchial secretion1 reports
laryngospasm1 reports
oxygen saturation decreased1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses: (†) Homeopathic remedy for general well being: defiance.

Dosage & Administration

Directions: (adults & children 6 years & older) Take 12 drops 2 times daily, or as recommended by your health care professional.

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.

Frequently Asked Questions

What is Emvita 7 used for?

Emvita 7 contains Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus. It is a liquid taken oral. Consult your doctor for specific uses.

Is Emvita 7 a controlled substance?

Emvita 7 is not classified as a controlled substance by the DEA.

What is the generic name for Emvita 7?

The generic name for Emvita 7 is Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus. There are no other listed brand versions of Anacard occ, Glandula sup, Lachesis mutus, Lycopodium, Phosphorus.

What is the NDC code for Emvita 7 18 [hp_M]/60mL?

The NDC (National Drug Code) for Emvita 7 18 [hp_M]/60mL is 66343-094, listed by RUBIMED AG.

Product NDC

66343-094

Package NDC

66343-094-60

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)