FDA.reportPublic FDA data

Lemon Quince

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:06:02

Label at a glance#

ProductLemon Quince
Active ingredientLEMON JUICE, QUINCE, BERBERIS VULGARIS ROOT BARK, SILICON DIOXIDE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: ONLY FOR USE AS A NASAL SPRAY.

DOSAGE & ADMINISTRATION SECTION

Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100 gm contains: 24 gm Citrus medica e succus 2X; Cydonia e fruct. 2X, Berberis e fruct 3X. Quartz 20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Aloe vera juice, Sodium chloride, Grapefruit seed extract

OTC - PURPOSE SECTION

Use: Temporary relief of nasal congestion and allergy 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 or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

SHAKE WELL BEFORE USE.
REFRIGERATE AFTER OPENING.
USE WITHIN 30 DAYS OF OPENING.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lemon Quince Nasal SprayLemon Quince Nasal Spray

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-608748951-6087-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRUS PARADISI SEED12F08874Y7IACT
LEMON JUICEAGN709ANTJACTIB
QUINCE12MCS4H09NACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB

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
2901b169-f493-820b-e063-6294a90a41ed15c1ac0f-1bcc-a167-e063-6294a90a03252024-12-11WarningsExact identifier
spl set id: 15c1ac0f-1bcc-a167-e063-6294a90a0325

Reported adverse events (FAERS/openFDA)#

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