CHAVITA 1- silicon dioxide, activated charcoal, urtica urens, frankincense, sus scrofa ovary, and bos taurus testicle 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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Chavita 1

Homeopathic Combination Medicine Indications: For menstrual and /or urinary discomfort

Ingredients

Silicea 21 x
Carbo veg. 50 C
Urtica urens 21 x
Olibanum 21 x
Ovary/Testis 21 x
Alcohol 51 % v/v

TAMPER-EVIDENT

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

Direction

12 drops two times per day or as directed by the practitioner.

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

Chavita 1

Homeopathic Combination
Medicine Indications:
For menstrual and/ or
urinary discomfort

RUBIMED®

1.7 Fl.oz. (50ml)

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

CHAVITA 1
silicon dioxide, activated charcoal, urtica urens, frankincense, sus scrofa ovary, and bos taurus testicle liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66343-006
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	21 [hp_X] in 1 mL
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	50 [hp_C] in 1 mL
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9)	URTICA URENS	21 [hp_X] in 1 mL
FRANKINCENSE (UNII: R9XLF1R1WM) (FRANKINCENSE - UNII:R9XLF1R1WM)	FRANKINCENSE	21 [hp_X] in 1 mL
SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O)	SUS SCROFA OVARY	21 [hp_X] in 1 mL
BOS TAURUS TESTICLE (UNII: PR4RXL6G2H) (BOS TAURUS TESTICLE - UNII:PR4RXL6G2H)	BOS TAURUS TESTICLE	21 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Alcohol (UNII: 3K9958V90M)	0.51 mL in 1 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66343-006-50	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

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

Labeler - RUBIMED AG (480582035)

Name	Address	ID/FEI	Business Operations
Establishment
RUBIMED AG		480582035	MANUFACTURE(66343-006)

Name	Address	ID/FEI	Business Operations
Establishment
Omida AG		483268348	MANUFACTURE(66343-006)