Viscum Quercus 1%

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:41

Label at a glance#

ProductViscum Quercus 1%
Active ingredientVISCUM ALBUM FRUITING TOP
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 Ingredient: Viscum album
(Quercus) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Sea
salt, Grapefruit seed extract

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ViscumQuercus1NasalSprayViscumQuercus1NasalSpray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9322-2Viscum Quercus 1%30 mL in 1 BOTTLE, SPRAYSPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9322VISCUM QUERCUS 1% SPRAY [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180514_6c2a8386-cb0a-745e-e053-2a91aa0af0af.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
48951-932248951-9322-2

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
6c2a8386-cb0b-745e-e053-2a91aa0af0af6c2a8386-cb0a-745e-e053-2a91aa0af0af2018-05-14WarningsExact identifier
spl id: 6c2a8386-cb0b-745e-e053-2a91aa0af0af
spl set id: 6c2a8386-cb0a-745e-e053-2a91aa0af0af

Reported adverse events (FAERS/openFDA)#

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