FDA.reportPublic FDA data

Emvita 12

Manufacturer
RUBIMED AG
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:13

Label at a glance#

ProductEmvita 12
Active ingredientAPIS MELLIFERA, BARIUM CARBONATE, ESCHSCHOLZIA CALIFORNICA WHOLE, GRAPHITE, STRYCHNOS IGNATII SEED, NAJA NAJA VENOM, BOS TAURUS THYMUS
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts Active Ingredients: (HPUS*) 14.3% of each

Apis mellifica 800C     Baryta carb 18LM
Eschscholtzia 21X      Graphites 21X
Ignatia 16LM             Naja 800C
Thymus gland 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.

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings:

Stop use if symptoms persist or worsen.

If you are pregnant or breastfeeding,consult a healthcare professional prior to use. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 

DOSAGE & ADMINISTRATION SECTION

Directions: (adults & children 6 years & older)

Take 12 drops 2 times daily, or as recommended by your health care professional. 

OTHER SAFETY INFORMATION

Other information: Store at 20 - 25°C

(68 - 77°F.) Do not use if box has been

tampered with, or if the safety seal of the

bottle is broken.

INACTIVE INGREDIENT SECTION

Inactive ingredients:Ethanol 20% USP,

Purified Water.

OTC - QUESTIONS SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 66343-099-60

RUBIMED

Emvita 12

Homeopathic Medicine For

General Well-being: 

Mental Overstrain

2.0 fl oz. 59mL 20% Ethanol

Emvita 12 - LabelEmvita 12 - Label

Emvita 12 - CartonEmvita 12 - Carton

OTC - PURPOSE SECTION

Homeopathic Medicine For

General Well-being:

Mental Overstain

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-099-60Emvita 1260 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-099EMVITA 12 (APIS MELLIFICA, BARYTA CARB, ESCHSCHOLTZIA, GRAPHITES, IGNATIA, NAJA, THYMUS GLAND) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_e6b25acc-0e84-45af-9e99-cb54695d5e71.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66343-09966343-099-60

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
APIS MELLIFERA7S82P3R43ZACTIB
BARIUM CARBONATE6P669D8HQ8ACTIB
ESCHSCHOLZIA CALIFORNICA WHOLE9315HN272XACTIB
GRAPHITE4QQN74LH4OACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
NAJA NAJA VENOMZZ4AG7L7VMACTIB
BOS TAURUS THYMUS8XEJ88V2T8ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Emvita 12APIS MELLIFICA, BARYTA CARB, ESCHSCHOLTZIA, GRAPHITES, IGNATIA, NAJA, THYMUS GLANDRUBIMED AGe6b25acc-0e84-45af-9e99-cb54695d5e712024-10-29WarningsExact identifier
ndc (package): 66343-099-60
ndc (product): 66343-099
ndc11 (package): 66343009960
spl id: 28173f16-e5a9-6a34-e063-6394a90a4642
spl set id: e6b25acc-0e84-45af-9e99-cb54695d5e71

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.