D-33

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 02:31:11

Label at a glance#

ProductD-33

Active ingredientATROPA BELLADONNA, BUFO BUFO CUTANEOUS GLAND, COPPER, ANEMONE PRATENSIS, SILICON DIOXIDE, ZINC

Label structure9 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0033-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Epilepsy, irritations of the nerve.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Belladonna 30x, Bufo rana 200x, Cuprum metallicum 12x, Pulsatilla 30x, Silicea 30x, Zincum metallicum 12x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

Rx CAUTION

PRECAUTIONS 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 33

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0033-1	2022-06-02	C162847	48780-1	9d75b9d0-7f57-f424-e053-dadaa90a57ce	D-33
58264-0033-1	2020-01-31	C162847	48780-1	9d75b9d0-7f57-f424-e053-dadaa90a57ce	D-33

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0033-1	D-33	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
58264-0033	D-33 (ATROPA BELLADONNA, BUFO BUFO CUTANEOUS GLAND, COPPER, ANEMONE PRATENSIS, SILICON DIOXIDE, AND ZINC) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250115_26f9bf6d-6038-42e8-b8c1-6c94ac4929af.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

D-33
ATROPA BELLADONNA, BUFO BUFO CUTANEOUS GLAND, COPPER, ANEMONE PRATENSIS, SILICON DIOXIDE, and ZINC
ALCOHOL
WATER
ATROPA BELLADONNA
BUFO BUFO CUTANEOUS GLAND
COPPER
ANEMONE PRATENSIS
SILICON DIOXIDE
ZINC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0033	58264-0033-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
ATROPA BELLADONNA	WQZ3G9PF0H	ACTIB
BUFO BUFO CUTANEOUS GLAND	Q59QU6N72Q	ACTIB
COPPER	789U1901C5	ACTIB
ANEMONE PRATENSIS	8E272251DI	ACTIB
SILICON DIOXIDE	ETJ7Z6XBU4	ACTIB
ZINC	J41CSQ7QDS	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-33	ATROPA BELLADONNA, BUFO BUFO CUTANEOUS GLAND, COPPER, ANEMONE PRATENSIS, SILICON DIOXIDE, AND ZINC	DNA Labs, Inc.	26f9bf6d-6038-42e8-b8c1-6c94ac4929af	2025-01-13	Warnings	Exact identifier ndc (package): 58264-0033-1 ndc (product): 58264-0033 ndc11 (package): 58264003301 spl id: 2b9eb825-2e83-846c-e063-6394a90a0a7b spl set id: 26f9bf6d-6038-42e8-b8c1-6c94ac4929af

Reported adverse events (FAERS/openFDA)#

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