CHAVITA 4- aur met, crataegus, cetraria, eucalyptus globulus, ferrum met, thymus gland, zinc val liquid

Chavita 4 by

Drug Labeling and Warnings

Chavita 4 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 21X        Crataegus 21X
Cetraria 21X        Eucalyptus globulus 21X
Ferrum met 50C  Thymus gland 21X
Zinc val 200C

*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 hay fever and allergies.

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: 66343-085-60

RUBIMED

Chavita 4

Homeopathic Medicine For

Hay Fever and Allergies

2.0 fl oz. 59mL 20% Ethanol

Homeopathic Medicine For

Hay Fever and Allergies

INGREDIENTS AND APPEARANCE

CHAVITA 4 
aur met, crataegus, cetraria, eucalyptus globulus, ferrum met, thymus gland, zinc val liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66343-085
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	21 [hp_X]  in 60 mL
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36)	HAWTHORN LEAF WITH FLOWER	21 [hp_X]  in 60 mL
CETRARIA ISLANDICA WHOLE (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA WHOLE - UNII:BJ7YPN79A1)	CETRARIA ISLANDICA WHOLE	21 [hp_X]  in 60 mL
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)	EUCALYPTUS GLOBULUS LEAF	21 [hp_X]  in 60 mL
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7)	IRON	50 [hp_C]  in 60 mL
BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (BOS TAURUS THYMUS - UNII:8XEJ88V2T8)	BOS TAURUS THYMUS	21 [hp_X]  in 60 mL
ZINC VALERATE DIHYDRATE (UNII: MN0RX54EQA) (VALERIC ACID - UNII:GZK92PJM7B)	ZINC VALERATE DIHYDRATE	200 [hp_C]  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: 66343-085-60	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)