D2

Manufacturer
DNA Labs, Inc.
Effective date
2018-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:12

Label at a glance#

ProductD2
Active ingredientGOLD TRICHLORIDE, CRATAEGUS LAEVIGATA WHOLE, SELENICEREUS GRANDIFLORUS WHOLE, DIBASIC POTASSIUM PHOSPHATE, ACONITUM NAPELLUS, VALERIANA OFFICINALIS WHOLE, SPIGELIA ANTHELMIA, ARNICA MONTANA, DIGITALIS PURPUREA WHOLE, PRUNUS LAUROCERASUS WHOLE, STRYCHNOS IGNATII WHOLE
Label structure9 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0002-1

INDICATIONS & USAGE SECTION

INDICATIONS

OTC - PURPOSE SECTION

Organic and functional affections of the heart.

OTC - ACTIVE INGREDIENT SECTION

INGREDIENTS

INACTIVE INGREDIENT SECTION

Aurum muriaticum 6x, Crataegus oxyacantha 1x, Cactus grandiflorus 4x, Kalium phosphoricum 4x, Aconitum napellus 6x, Valeriana officinalis 3x, Spigelia anthelmia 4x, Arnica montana 4x, Digitalis purpurea 4x, Laurocerasus 4x, Ignatia amara 4x, 20% alcohol in purified water.

Rx CAUTION

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without a prescription.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper full under the tongue two times daily. In acute conditions 5-10 drops under the tongue every 20-30 minutes.

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

  • As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

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.

D2

HOMEOPATHIC FORMULA

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
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0002-12020-01-31C16284748780-19d75b9d0-c0e8-f424-e053-dadaa90a57ceD2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0002-1D229.57 mL in 1 BOTTLE, GLASSSOLUTION29.571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0002D2 (GOLD TRICHLORIDE, CRATAEGUS LAEVIGATA WHOLE, SELENICEREUS GRANDIFLORUS WHOLE, DIBASIC POTASSIUM PHOSPHATE, ACONITUM NAPELLUS, VALERIANA OFFICINALIS WHOLE, SPIGELIA ANTHELMIA, ARNICA MONTANA, DIGITALIS PURPUREA WHOLE, PRUNUS LAUROCERASUS WHOLE, AND STRYCHNOS IGNATII WHOLE) SOLUTION [DNA LABS, INC.]1Legacy NDC, 1 package rows20180202_146b1277-28c3-43e3-877b-13b324717d2a.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-000258264-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
908e4ffc-c159-41ba-97ff-5e972fb82195146b1277-28c3-43e3-877b-13b324717d2a2018-01-31WarningsExact identifier
spl id: 908e4ffc-c159-41ba-97ff-5e972fb82195
spl set id: 146b1277-28c3-43e3-877b-13b324717d2a

Reported adverse events (FAERS/openFDA)#

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