FDA.reportPublic FDA data

A-10

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:30:12

Label at a glance#

ProductA-10
Active ingredientQUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, QUERCUS GARRYANA WHOLE
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0302-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Allergies.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Oak

SPL UNCLASSIFIED SECTION

Red 6/12/30x, Black 6/12/30x, White 6/12/30x, California black 6/12/30x, California live 6/12/30x, Western white 6/12/30x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

Normal dose for the first week is 2-3 drops in water T.I.D. Add one drop per dose per week until a total of ten drops is reached.

STORAGE AND HANDLING SECTION

SHAKE WELL

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

  • Use only if cap seal is unbroken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep this and all medication out of the reach of children.

SPL UNCLASSIFIED SECTION

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

A-10
EASTERN-WESTERN
OAK MIX

HOMEOPATHIC ANTIGEN

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0302-12022-05-30C16284748780-19d75b9cf-fa0d-f424-e053-dadaa90a57ceA-10
58264-0302-12020-01-31C16284748780-19d75b9cf-fa0d-f424-e053-dadaa90a57ceA-10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0302-1A-1029.57 mL in 1 BOTTLE, GLASSSOLUTION29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0302A-10 (QUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, AND QUERCUS GARRYANA WHOLE) SOLUTION [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250112_136b0cf9-3725-41c0-9f81-65ca5cc48abe.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-030258264-0302-1

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
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
QUERCUS RUBRA WHOLEUQ0Z34X16UACTIB
QUERCUS VELUTINA WHOLE3NQP837A96ACTIB
QUERCUS ALBA WOODXR6BC2ZUAMACTIB
QUERCUS KELLOGGII WHOLENM384AFV9HACTIB
QUERCUS AGRIFOLIA WHOLE29104Z8OW7ACTIB
QUERCUS GARRYANA WHOLE9E9919P3GNACTIB

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
A-10QUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, AND QUERCUS GARRYANA WHOLEDNA Labs, Inc.136b0cf9-3725-41c0-9f81-65ca5cc48abe2025-01-09WarningsExact identifier
ndc (package): 58264-0302-1
ndc (product): 58264-0302
ndc11 (package): 58264030201
spl id: 2b4df692-11f1-153c-e063-6294a90abc32
spl set id: 136b0cf9-3725-41c0-9f81-65ca5cc48abe

Reported adverse events (FAERS/openFDA)#

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