FDA.reportPublic FDA data

Emvita 21

Manufacturer
RUBIMED AG
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:09

Label at a glance#

ProductEmvita 21
Active ingredientARSENIC TRIOXIDE, MATRICARIA CHAMOMILLA WHOLE, SUS SCROFA PITUITARY GLAND, LACHESIS MUTA VENOM, MAGNESIUM CARBONATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts Active Ingredients: (HPUS*) 20% of each

Arsenicum alb 21X   Chamomilla 18LM
Hypophysis 21X       Lachesis mutus 800C
Mag carb 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: physical 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 66343-108-60

RUBIMED

Emvita 21

Homeopathic Medicine For

General Well-being: 

Physical Overstrain

2.0 fl oz. 59mL 20% Ethanol

Emvita 21 - LabelEmvita 21 - Label

Emvita 21 - CartonEmvita 21 - Carton

OTC - PURPOSE SECTION

Homeopathic Medicine For

General Well-being:

Physical Overstrain

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66343-108-60Emvita 2160 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66343-108EMVITA 21 (ARSENICUM ALB, CHAMOMILLA, HYPOPHYSIS, LACHESIS MUTUS, MAG CARB) LIQUID [RUBIMED AG]2Current NDC, Legacy NDC, 1 package rows20241201_46ddfe55-5189-4e43-9e30-44a33bb4a7a7.zip

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
66343-10866343-108-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARSENIC TRIOXIDES7V92P67HOACTIB
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZACTIB
SUS SCROFA PITUITARY GLANDL0PFEMQ1DTACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
MAGNESIUM CARBONATE0E53J927NAACTIB

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 21ARSENICUM ALB, CHAMOMILLA, HYPOPHYSIS, LACHESIS MUTUS, MAG CARBRUBIMED AG46ddfe55-5189-4e43-9e30-44a33bb4a7a72024-10-29WarningsExact identifier
ndc (package): 66343-108-60
ndc (product): 66343-108
ndc11 (package): 66343010860
spl id: 281773be-dcf8-eed9-e063-6394a90a1052
spl set id: 46ddfe55-5189-4e43-9e30-44a33bb4a7a7

Reported adverse events (FAERS/openFDA)#

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