ANXIOVITA- aconitum napellus, anacardium orientale, cerebrum, hypericum perforatum liquid

Anxiovita by

Drug Labeling and Warnings

Anxiovita by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

Aconitum napellus 18LM

Anacardium orientale 12X

Cerebrum 200C

Hypericum perforatum 21X

*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE

​Uses: ​(†) Homeopathic remedy to alleviate

Anxiety   Nervousness   Stress

WARNINGS

​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.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

​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 - 25°C

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

tampered with, or is the safety seal of the

bottle is broken.

INACTIVE INGREDIENT

​inactive ingredients: ​Ethanol 20% USP,

Purified Water.

QUESTIONS

Manufactured by: OHM pharma, Inc, USA.

Distributed by: Privia Naturals, LLC.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

www.priviannaturals.com

1 (888) 526-9695 Product of USA.

PRINCIPAL DISPLAY PANEL

​NDC: 66343-042-50

RUBIMED

Anxiovita

Homeopathic Medicine For

Anxiety, Nervousness & Stress

​​1.7 fl oz. 50 mL  20% Ethanol

​Homeopathic Medicine For

Anxiety, Nervousness & Stress

INGREDIENTS AND APPEARANCE

ANXIOVITA 
aconitum napellus, anacardium orientale, cerebrum, hypericum perforatum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-042
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	18 [hp_M]  in 50 mL
SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (SEMECARPUS ANACARDIUM JUICE - UNII:Y0F0BU8RDU)	SEMECARPUS ANACARDIUM JUICE	12 [hp_X]  in 50 mL
SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532)	SUS SCROFA CEREBRUM	200 [hp_C]  in 50 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	21 [hp_X]  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-042-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/03/2019

Labeler - RUBIMED AG (480582035)