Fragaria Vitis by Uriel Pharmacy, Inc FRAGARIA VITIS tablet

Fragaria Vitis by

Drug Labeling and Warnings

Fragaria Vitis 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: 1-2 tablets.

Ages 2-11: 1 tablet. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Fragaria vesca e fol. (Wild strawberry leaf) 1X double strength, Vitis vinifera e fol. (Grape vine leaf) 1X double strength

INACTIVE INGREDIENT

Inactive Ingredients: Emdex, Magnesium stearate

Prepared using rhythmical processes.

PURPOSE

Use: Supports normal liver function.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence.
Not FDA evaluated. 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.

QUESTIONS

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FRAGARIA VITIS 
fragaria vitis tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-4189
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	1 [hp_X]
VITIS VINIFERA LEAF (UNII: R1H893D80E) (VITIS VINIFERA LEAF - UNII:R1H893D80E)	VITIS VINIFERA LEAF	1 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
DEXTRATES (UNII: G263MI44RU)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	brown	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-4189-4	50 in 1 BOTTLE, GLASS; 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(48951-4189)