FDA.reportPublic FDA data

A-26

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 02:30:11

Label at a glance#

ProductA-26
Active ingredientARTEMISIA LUDOVICIANA POLLEN, ARTEMISIA TRIDENTATA POLLEN
Label structure7 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0318-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Allergies.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Prairie 6/12/30x, Common 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.

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-26
SAGE 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
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0318-12022-05-30C16284748780-19d75b9d0-2488-f424-e053-dadaa90a57ceA-26
58264-0318-12020-01-31C16284748780-19d75b9d0-2488-f424-e053-dadaa90a57ceA-26

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0318-1A-2629.57 mL in 1 BOTTLE, GLASSSOLUTION29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0318A-26 (ARTEMISIA LUDOVICIANA POLLEN AND ARTEMISIA TRIDENTATA POLLEN) SOLUTION [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250112_05d2a686-a421-4f66-b634-cf42fc96868b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-031858264-0318-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARTEMISIA LUDOVICIANA POLLEN57KIJ4772HACTIB
ARTEMISIA TRIDENTATA POLLENYI19RB8YFDACTIB

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-26ARTEMISIA LUDOVICIANA POLLEN AND ARTEMISIA TRIDENTATA POLLENDNA Labs, Inc.05d2a686-a421-4f66-b634-cf42fc96868b2025-01-09WarningsExact identifier
ndc (package): 58264-0318-1
ndc (product): 58264-0318
ndc11 (package): 58264031801
spl id: 2b50d137-37da-851a-e063-6294a90a0a4d
spl set id: 05d2a686-a421-4f66-b634-cf42fc96868b

Reported adverse events (FAERS/openFDA)#

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