Fragaria Vitis

Manufacturer
Uriel Pharmacy Inc
Effective date
2024-09-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:27:53

Label at a glance#

ProductFragaria Vitis
Active ingredientVITIS VINIFERA LEAF, FRAGARIA VESCA WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Fragaria e fol. (Strawberry Leaf) 2X, Vitis e fol. (Grape vine) 2X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Propolis

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Supports normal liver function.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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.

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

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fragaria Vitis LiquidFragaria Vitis Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4169-3Fragaria Vitis60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4169FRAGARIA VITIS LIQUID [URIEL PHARMACY INC]3Legacy NDC, 1 package rows20240905_d321ce4e-ae9d-7c75-e053-2a95a90ae2e1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-416948951-4169-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
213ab6e6-efde-ddb5-e063-6394a90a8a6ad321ce4e-ae9d-7c75-e053-2a95a90ae2e12024-09-03WarningsExact identifier
spl id: 213ab6e6-efde-ddb5-e063-6394a90a8a6a
spl set id: d321ce4e-ae9d-7c75-e053-2a95a90ae2e1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.