D-39

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 02:31:09

Label at a glance#

ProductD-39

Active ingredientLACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, VESPA CRABRO

Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0039-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Supports ovary on the left side.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Lachesis mutus 30x, Lycopodium clavatum 30x, Palladium metallicum 12x, Saxifraga granulata 30x, Vespa crabro 12x

INACTIVE

INACTIVE INGREDIENT SECTION

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

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 39

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0039-1	2022-06-02	C162847	48780-1	9d75b9d0-d594-f424-e053-dadaa90a57ce	D-39
58264-0039-1	2020-01-31	C162847	48780-1	9d75b9d0-d594-f424-e053-dadaa90a57ce	D-39

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0039-1	D-39	29.57 mL in 1 BOTTLE, GLASS	SOLUTION	29.57		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58264-0039	D-39 (LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, AND VESPA CRABRO) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250115_0d997878-b973-45aa-a319-9194fcecc5fc.zip

Products#

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

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

D-39
LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, and Vespa crabro
ALCOHOL
WATER
LACHESIS MUTA VENOM
LYCOPODIUM CLAVATUM SPORE
PALLADIUM
SAXIFRAGA GRANULATA WHOLE
VESPA CRABRO

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0039	58264-0039-1

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
LACHESIS MUTA VENOM	VSW71SS07I	ACTIB
LYCOPODIUM CLAVATUM SPORE	C88X29Y479	ACTIB
PALLADIUM	5TWQ1V240M	ACTIB
SAXIFRAGA GRANULATA WHOLE	W1LUS9R48G	ACTIB
VESPA CRABRO	K3ALM8S49H	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
D-39	LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, PALLADIUM, SAXIFRAGA GRANULATA WHOLE, AND VESPA CRABRO	DNA Labs, Inc.	0d997878-b973-45aa-a319-9194fcecc5fc	2025-01-13	Warnings	Exact identifier ndc (package): 58264-0039-1 ndc (product): 58264-0039 ndc11 (package): 58264003901 spl id: 2b9ecbda-7107-d64a-e063-6294a90aac9e spl set id: 0d997878-b973-45aa-a319-9194fcecc5fc

Reported adverse events (FAERS/openFDA)#

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