FDA.reportPublic FDA data

D-104

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:31:08

Label at a glance#

ProductD-104
Active ingredientAPIUM GRAVEOLENS WHOLE, ASCLEPIAS INCARNATA ROOT, CALCIUM ARSENATE, CAMPHOR (NATURAL), ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHRASIA STRICTA, FERROUS IODIDE, ICHTHAMMOL, SCABIES LESION LYSATE (HUMAN), THUJA OCCIDENTALIS LEAFY TWIG, TRIFOLIUM REPENS FLOWER
Label structure9 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0110-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For viral infections.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Apium graveolens 6x 12x, Asclepias incarnata 4x, Calcarea arsenicosa 12x, 30x, Camphora 12x, 30x, Echinacea angustifolia 4x, Eupatorium perfoliatum 6x, 12x, 30x, Euphrasia officinalis 6x, 12x, Ferrum iodatum 6x, 12x, Icthyolum 12x, 30x, Psorinum 30x, Thuja occidentalis 6x, 12x, 30x, Trifolium repens 4x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

Rx CAUTION

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without a prescription.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

STORAGE AND HANDLING SECTION

SHAKE WELL

Warnings

WARNINGS 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.

D 104

HOMEOPATHIC
STRESS 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
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0110-12022-06-06C16284748780-19d75b9d0-9112-f424-e053-dadaa90a57ceD-104
58264-0110-12020-01-31C16284748780-19d75b9d0-9112-f424-e053-dadaa90a57ceD-104

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0110-1D-10429.57 mL in 1 BOTTLE, GLASSSOLUTION29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0110D-104 (APIUM GRAVEOLENS WHOLE, ASCLEPIAS INCARNATA ROOT, CALCIUM ARSENATE, CAMPHOR (NATURAL), ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHRASIA STRICTA, FERROUS IODIDE, ICHTHAMMOL, SCABIES LESION LYSATE (HUMAN), THUJA OCCIDENTALIS LEAFY TWIG, AND TRIFOLIUM REPENS FLOWER) SOLUTION [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250115_09c3912a-71ba-4814-8b91-d0e787b542bf.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
58264-011058264-0110-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
APIUM GRAVEOLENS WHOLE15V0BLB71GACTIB
ASCLEPIAS INCARNATA ROOT4N9UU1HQKGACTIB
CALCIUM ARSENATE95OX15I8ZUACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
FERROUS IODIDEF5452U54PNACTIB
ICHTHAMMOLNQ14646378ACTIB
SCABIES LESION LYSATE (HUMAN)5UAU16Z1U4ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
TRIFOLIUM REPENS FLOWER49Y788T742ACTIB

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
D-104APIUM GRAVEOLENS WHOLE, ASCLEPIAS INCARNATA ROOT, CALCIUM ARSENATE, CAMPHOR (NATURAL), ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHRASIA STRICTA, FERROUS IODIDE, ICHTHAMMOL, SCABIES LESION LYSATE (HUMAN), THUJA OCCIDENTALIS LEAFY TWIG, AND TRIFOLIUM REPENS FLOWERDNA Labs, Inc.09c3912a-71ba-4814-8b91-d0e787b542bf2025-01-13WarningsExact identifier
ndc (package): 58264-0110-1
ndc (product): 58264-0110
ndc11 (package): 58264011001
spl id: 2b9ed194-def5-363e-e063-6294a90a8cdc
spl set id: 09c3912a-71ba-4814-8b91-d0e787b542bf

Reported adverse events (FAERS/openFDA)#

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