Anxiovita

Drug Labeling and Warnings

Drug Details [pdf]

ANXIOVITA- piper methysticum root, hypericum perforatum, sus scrofa cerebellum, and aconitum napellus liquid 
RUBIMED AG

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Anxiovita

Homeopathic Combination Medicine Indications: For feeling frightened

Ingredients

Piper methysiicum 12 x
Hypericum 21 x
Cerebellum suis 200 C
Aconitum napellus 18 LM
Alcohol 44% v/v

TAMPER-EVIDENT

Do not use this product if seal at base of cap is missing or broken.

Direction

10 drops per day or as instructed by your health care provider.

Warnings

As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using the product.

Keep out of Reach of Children!

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

Anxiovita

Homeopathic Combination
Medicine Indications:
For feeling frightened

RUBIMED®

1.7 Fl.oz. (50ml)

ANXIOVITA 
piper methysticum root, hypericum perforatum, sus scrofa cerebellum, and aconitum napellus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PIPER METHYSTICUM ROOT (UNII: BOW48C81XP) (PIPER METHYSTICUM ROOT - UNII:BOW48C81XP)	PIPER METHYSTICUM ROOT	12 [hp_X]  in 1 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	21 [hp_X]  in 1 mL
SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (SUS SCROFA CEREBELLUM - UNII:49NGK53TPQ)	SUS SCROFA CEREBELLUM	200 [hp_C]  in 1 mL
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	18 [hp_M]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)	0.44 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66343-001-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/07/2019	07/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved homeopathic		05/07/2015	07/01/2019

Labeler - RUBIMED AG (480582035)

Revised: 7/2019

Document Id: 724b2731-4d76-4b6b-9edf-a0ea82d17aa7

34390-5

Set id: f135c591-e308-4d1e-b478-b08373fd8f3a

Version: 2

Effective Time: 20190718

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