T-39

Manufacturer: DNA Labs, Inc.
Effective date: 2025-01-09
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:30:15

Label at a glance#

ProductT-39

Active ingredientORNITHOGALUM UMBELLATUM, HELIANTHEMUM NUMMULARIUM WHOLE, IMPATIENS GLANDULIFERA WHOLE, PRUNUS CERASIFERA WHOLE, CLEMATIS VITALBA WHOLE

Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0284-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

All purpose remedy for terror, shock, emotional upset, "stage fright", etc.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

Ornithogalum umbellatum 6/8/30x, Helianthemum nummularium 6/8/30x, Impatiens glandulifera 6/8/30x, Prunus cerasifera 6/8/30x, Clematis vitalba 6/8/30x, 20% alcohol in purified water.

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

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.

T-39

EMOTIONAL
EMERGENCY

FLOWER ESSENCES

1 FL. OZ.

T-39 DIST Label Proof 4.22jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0284-1	2020-01-31	C162847	48780-1	9d75b9d0-69f1-f424-e053-dadaa90a57ce	T-39

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0284-1	T-39	29.57 mL in 1 BOTTLE, GLASS	SOLUTION	29.57		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58264-0284	T-39 (ORNITHOGALUM UMBELLATUM, HELIANTHEMUM NUMMULARIUM WHOLE, IMPATIENS GLANDULIFERA WHOLE, PRUNUS CERASIFERA WHOLE, AND CLEMATIS VITALBA WHOLE) SOLUTION [DNA LABS, INC.]	5	Current NDC, Legacy NDC, 1 package rows	20250112_31c43f09-f24f-4343-8b9c-86c52e1966c0.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

T-39
Ornithogalum umbellatum, Helianthemum nummularium whole, Impatiens glandulifera whole, Prunus cerasifera whole, and Clematis vitalba whole
ALCOHOL
WATER
ORNITHOGALUM UMBELLATUM
HELIANTHEMUM NUMMULARIUM WHOLE
IMPATIENS GLANDULIFERA WHOLE
PRUNUS CERASIFERA WHOLE
CLEMATIS VITALBA WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0284	58264-0284-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
ORNITHOGALUM UMBELLATUM	9NS3M2Y78S	ACTIB
HELIANTHEMUM NUMMULARIUM WHOLE	R0G6QEU3M0	ACTIB
IMPATIENS GLANDULIFERA WHOLE	21L92F0HMH	ACTIB
PRUNUS CERASIFERA WHOLE	XVE14FEG0K	ACTIB
CLEMATIS VITALBA WHOLE	7PH07Z124Q	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
T-39	ORNITHOGALUM UMBELLATUM, HELIANTHEMUM NUMMULARIUM WHOLE, IMPATIENS GLANDULIFERA WHOLE, PRUNUS CERASIFERA WHOLE, AND CLEMATIS VITALBA WHOLE	DNA Labs, Inc.	31c43f09-f24f-4343-8b9c-86c52e1966c0	2025-01-09	Warnings	Exact identifier ndc (package): 58264-0284-1 ndc (product): 58264-0284 ndc11 (package): 58264028401 spl id: 2b53e2b9-4877-a32a-e063-6294a90a0ebe spl set id: 31c43f09-f24f-4343-8b9c-86c52e1966c0

Reported adverse events (FAERS/openFDA)#

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