FDA.reportPublic FDA data

Quercus Borago

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:30:07

Label at a glance#

ProductQuercus Borago
Active ingredientHORSE CHESTNUT, QUERCUS ROBUR WHOLE, MERCURIALIS PERENNIS, BORAGE, MILK THISTLE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ANTIMONY
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100 gm contains: 10 gm Quercus (Oak) 1X, 1 gm Mercurialis per. (Dog’s mercury) 1X, 0.5 gm Aesculus (Horse chestnut) 1X, 0.5 gm Borago (Borage) 1X, 0.5 gm Carduus marianus (Milk thistle) 1X, 0.5 gm Hamamelis (Witch hazel) 1X; 0.1gm Stibium met. (Antimony) 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Lanolin Anhydrous, Spring water, Distilled water, Beeswax, Mineral oil, Sorbic acid, Tea tree oil, Grapefruit seed extract

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of hemorrhoid symptoms.

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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. 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

Quercus Borago OintmentQuercus Borago Ointment

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8352-5Quercus Borago60 g in 1 TUBEOINTMENT604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8352QUERCUS BORAGO OINTMENT [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 1 package rows20250109_8243228b-89ec-2b53-e053-2a91aa0a0f38.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-835248951-8352-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
OLIVE OIL6UYK2W1W1EIACT
WATER059QF0KO0RIACT
LANOLIN7EV65EAW6HIACT
YELLOW WAX2ZA36H0S2VIACT
MINERAL OILT5L8T28FGPIACT
HORSE CHESTNUT3C18L6RJAZACTIB
CITRUS PARADISI SEED12F08874Y7IACT
QUERCUS ROBUR WHOLER7QMG0BT2WACTIB
MERCURIALIS PERENNISQ35465A1MAACTIB
BORAGEPB618V0K2WACTIB
MILK THISTLEU946SH95EEACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB
ANTIMONY9IT35J3UV3ACTIB
TEA TREE OILVIF565UC2GIACT
SORBIC ACIDX045WJ989BIACT

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
Quercus BoragoQUERCUS BORAGOUriel Pharmacy Inc.8243228b-89ec-2b53-e053-2a91aa0a0f382025-01-07WarningsExact identifier
ndc (package): 48951-8352-5
ndc (product): 48951-8352
ndc11 (package): 48951835205
spl id: 2b246ce3-513b-97aa-e063-6294a90a95dc
spl set id: 8243228b-89ec-2b53-e053-2a91aa0a0f38

Reported adverse events (FAERS/openFDA)#

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