Quercus Rubra Glandium

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2016-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:28

Label at a glance#

ProductQuercus Rubra Glandium
Active ingredientQUERCUS RUBRA WHOLE
Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-17.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

imgimg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-666-012020-01-31C16284748780-19d75b9d0-703c-f424-e053-dadaa90a57ce44bdd485-709c-28a1-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-666-01Quercus Rubra Glandium240 [hp_C] in 1 VIAL, GLASSPELLET2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-666QUERCUS RUBRA GLANDIUM PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 1 package rows20161229_44bdd485-709c-28a1-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63545-66663545-666-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
QUERCUS RUBRA WHOLEUQ0Z34X16UACTIB
SUCROSEC151H8M554IACT

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
44bdd485-709d-28a1-e054-00144ff88e8844bdd485-709c-28a1-e054-00144ff88e882016-12-28Exact identifier
spl id: 44bdd485-709d-28a1-e054-00144ff88e88
spl set id: 44bdd485-709c-28a1-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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