ARCTOSTAPHYLOS UVA-URSI LEAF

Manufacturer: Uriel Pharmacy, Inc
Effective date: 2025-01-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:31:29

Label at a glance#

ProductUva ursi comp.

Active ingredientARCTOSTAPHYLOS UVA-URSI LEAF, WORMWOOD, BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, LARIX DECIDUA RESIN

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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: Absinthium ex herba infusion (Wormwood) 1X, Berberis e fruct (Barberry) 1X, Uva ursi Dec (Bearberry) 1X, Cantharis (Spanish fly) 2X, Resina laricis (Larch resin) 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 30% Organic cane alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of urinary discomfort.

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.

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

Uva ursi comp. Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-9389-3	Uva ursi comp.	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-9389	UVA URSI COMP. LIQUID [URIEL PHARMACY, INC]	1	Current NDC, 1 package rows	20250121_2c280a05-da87-0480-e063-6294a90a9502.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Uva ursi comp.
ARCTOSTAPHYLOS UVA-URSI LEAF
WORMWOOD
ALCOHOL
BERBERIS VULGARIS ROOT BARK
LYTTA VESICATORIA
WATER
LARIX DECIDUA RESIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-9389	48951-9389-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARCTOSTAPHYLOS UVA-URSI LEAF	3M5V3D1X36	ACTIB
WORMWOOD	F84709P2XV	ACTIB
ALCOHOL	3K9958V90M	IACT
BERBERIS VULGARIS ROOT BARK	1TH8Q20J0U	ACTIB
LYTTA VESICATORIA	3Q034RO3BT	ACTIB
WATER	059QF0KO0R	IACT
LARIX DECIDUA RESIN	AD8LJ73GQF	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Uva ursi comp.	UVA URSI COMP.	Uriel Pharmacy, Inc	2c280a05-da87-0480-e063-6294a90a9502	2025-01-20	Warnings	Exact identifier ndc (package): 48951-9389-3 ndc (product): 48951-9389 ndc11 (package): 48951938903 spl id: 2c280a05-da88-0480-e063-6294a90a9502 spl set id: 2c280a05-da87-0480-e063-6294a90a9502

Reported adverse events (FAERS/openFDA)#

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