FRAGARIA VITIS LIQUID liquid

Fragaria Vitis Liquid by

Drug Labeling and Warnings

Fragaria Vitis Liquid by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Grape leaf extract, Strawberry leaf extract

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Propolis

PURPOSE

Use: Supports normal liver function.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 30 DAYS OF OPENING.

*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FRAGARIA VITIS LIQUID 
fragaria vitis liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-4160
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FRAGARIA VESCA WHOLE (UNII: 5J340B7H82) (FRAGARIA VESCA WHOLE - UNII:5J340B7H82)	FRAGARIA VESCA WHOLE	2 [hp_X]  in 1 mL
HONEY (UNII: Y9H1V576FH) (HONEY - UNII:Y9H1V576FH)	HONEY	2 [hp_X]  in 1 mL
VITIS VINIFERA LEAF (UNII: R1H893D80E) (VITIS VINIFERA LEAF - UNII:R1H893D80E)	VITIS VINIFERA LEAF	2 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-4160-3	60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc.		043471163	manufacture(48951-4160)