CHAVITA 7- aur met, calc sulf, cerebrum, hypericum perforatum, lachesis mutus, millefolium, valeriana liquid

Chavita 7 by

Drug Labeling and Warnings

Chavita 7 by is a Homeopathic medication manufactured, distributed, or labeled by RUBIMED AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts Active Ingredients: (HPUS*) 14.3% of each

Aur met 200C            Calc sulf 200C
Cerebrum 21X           Hypericum perforatum 21X
Lachesis mutus 21X   Millefolium 21X
Valeriana 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

Uses: (†) Homeopathic remedy for dizziness.

WARNINGS

Warnings:

Stop use if symptoms persist or worsen.

If you are pregnant or breastfeeding,consult a healthcare professional prior to use. 

Keep out of reach of children. 

DOSAGE & ADMINISTRATION

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

Inactive ingredients:Ethanol 20% USP,

Purified Water.

QUESTIONS

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.

PRINCIPAL DISPLAY PANEL

NDC: 66343-088-60

RUBIMED

Chavita 7

Homeopathic Medicine For

Dizziness

2.0 fl oz. 59mL 20% Ethanol

Homeopathic Medicine For

Dizziness

INGREDIENTS AND APPEARANCE

CHAVITA 7 
aur met, calc sulf, cerebrum, hypericum perforatum, lachesis mutus, millefolium, valeriana liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-088
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	200 [hp_C]  in 60 mL
CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE ANHYDROUS	200 [hp_C]  in 60 mL
SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532)	SUS SCROFA CEREBRUM	21 [hp_X]  in 60 mL
HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM WHOLE	21 [hp_X]  in 60 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	21 [hp_X]  in 60 mL
ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK)	ACHILLEA MILLEFOLIUM WHOLE	21 [hp_X]  in 60 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	21 [hp_X]  in 60 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: 66343-088-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/19/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/01/2022

Labeler - RUBIMED AG (480582035)