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

Pharmacopoedia 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 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 - 25ºC

(68 - 77ºF). 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.

197 Woodland Pkwy Suite 104 #813

San Marcos, CA 92069

www.privianaturals.com

1 (888) 526-9695 Product of USA.

PRINCIPAL DISPLAY PANEL

​NDC: 66343-049-50

RUBIMED

Chavita 7

​​Homeopathic Medicine For

Dizziness

1.7 fl oz.  50 mL  20% Ethanol

​Homeopathic Medicine For

Dizziness

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 66343-049
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 50 mL
SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532)	SUS SCROFA CEREBRUM	21 [hp_X]  in 50 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	21 [hp_X]  in 50 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	21 [hp_X]  in 50 mL
CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE ANHYDROUS	200 [hp_C]  in 50 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	21 [hp_X]  in 50 mL
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK)	ACHILLEA MILLEFOLIUM	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: 66343-049-50	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)