FDA.reportPublic FDA data

Viscum Quercus 1%

Product NDC
48951-9322
11-digit product format
489519322
Labeler code
48951
Product ID
48951-9322_6c2a8386-cb0b-745e-e053-2a91aa0af0af
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Quercus 1%
Dosage form
SPRAY
Route
NASAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
VISCUM ALBUM FRUITING TOP
Active strength
1 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-9322IInactivated by FDA2026-10-05
excluded packagepackage48951-932248951-9322-2IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

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

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9322-24895193220230 mL in 1 BOTTLE, SPRAY (48951-9322-2) 30 ml2009-09-010000-00-00NoNoCurrent