Emvita 12

Manufacturer
RUBIMED AG
Effective date
2021-01-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:55:42

Label at a glance#

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredients: ​14.3% of each

Apis mellifica 800C         Baryta carb 18LM

Eschscholtzia 21X        Graphites 21X

Ignatia 16LM             Naja 800C

Thymus gland

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

INDICATIONS & USAGE SECTION

​Uses: ​(†) Homeopathic remedy for mental

overexertion.

WARNINGS SECTION

​Warnings:

Stop use if symptoms persist or worsen.

​If you area pregnant or breastfeeding,

​consult a health care professional prior to use.

​Keep ​ ​out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

​Directions: ​(adults & children 6 years & older)

Take 5 drops 3 - 6 times daily, or as

recommended by your health care

professional.

OTHER SAFETY INFORMATION

​Other information:​ Store at 20 - 25ºC

(68 - 77ºF). 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.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​NDC 66343-061-50

RUBIMED

Emvita 12

1.7 fl oz. Bottle Label1.7 fl oz. Bottle Label

​Homeopathic Medicine For

​Mental Overexertion

​1.7 fl oz. 50 mL    20% Ethanol

OTC - PURPOSE SECTION

Homeopathic remedy for mental

overexertion.

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66343-06166343-061-50

Ingredients#

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

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

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
c19cd50c-a29c-41a1-ba9e-0cfdffb0d1f4c764448e-5cce-4e92-beeb-971caace26dd2022-01-05WarningsExact identifier
spl set id: c764448e-5cce-4e92-beeb-971caace26dd

Reported adverse events (FAERS/openFDA)#

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