Paravita

Manufacturer
RUBIMED AG
Effective date
2021-01-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:55:39

Label at a glance#

ProductParavita
Active ingredientSUS SCROFA CEREBRUM, FORMICA RUFA, SULFUR, VESPA CRABRO
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Drug Facts

​Active Ingredients: ​(HPUS*) 25% of each

Cerebrum 21X

Formica rufa 12X

Sulphur 200C

Vespa crabro 30X

*The letters "HPUS" indicate that the

components in this product are officially

monographed in the Homeopathic

Pharmacopoeia of the Untied States.

†Claims based on traditional homeopathic

practice, not accepted medical evidence. Not

FDA evaluated.

INDICATIONS & USAGE SECTION

​Uses:​ (†) Homeopathic remedy to 

rebalance the autonomic regulation.

WARNINGS SECTION

​Warnings:

​Stop use if symptoms persist or worsen.

​If you are 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

www.privianaturals.com

1 (888) 526-9695 Product of USA.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​NDC 66343-080-50

RUBIMED

Paravita

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

​Homeopathic Medicine To

​Rebalance The Autonomic

​Regulation

​1.7 fl oz. 50 mL    20% Ethanol

OTC - PURPOSE SECTION

Homeopathic Medicine To

Rebalance The Autonomic

Regulation

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66343-08066343-080-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
cde289cb-603a-404f-90bf-7cb48335c58aa55ba520-8bf0-4092-9c1c-1850bf0a67cd2022-01-06WarningsExact identifier
spl set id: a55ba520-8bf0-4092-9c1c-1850bf0a67cd

Reported adverse events (FAERS/openFDA)#

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