FDA.reportPublic FDA data

D-67

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-67
Active ingredientAMMONIUM CARBONATE, HYDROGEN CYANIDE, CAMPHOR (NATURAL), ACTIVATED CHARCOAL, CROTALUS DURISSUS TERRIFICUS VENOM, TOBACCO LEAF, VERATRUM ALBUM ROOT, SPIGELIA ANTHELMIA
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0067-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Supports healthy circulation.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Ammonium carbonicum 6x, Acidum hydrocyanicum 6x, Camphora 4x, Carbo vegetabilis 30x, Crotalus cascavella 12x, Tabacum 6x, Veratrum album 4x, Spigelia anthelmia 6x

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 67

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0067-12022-06-03C16284748780-19d75b9d0-ab85-f424-e053-dadaa90a57ceD-67
58264-0067-12020-01-31C16284748780-19d75b9d0-ab85-f424-e053-dadaa90a57ceD-67

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0067-1D-6729.57 mL in 1 BOTTLE, GLASSSOLUTION29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0067D-67 (AMMONIUM CARBONATE, HYDROGEN CYANIDE, CAMPHOR (NATURAL), ACTIVATED CHARCOAL, CROTALUS DURISSUS TERRIFICUS VENOM, TOBACCO LEAF, VERATRUM ALBUM ROOT, AND SPIGELIA ANTHELMIA) SOLUTION [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250115_202cdebf-12a1-485a-9bd6-05f5eb745dbf.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-006758264-0067-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
AMMONIUM CARBONATENJ5VT0FKLJACTIB
HYDROGEN CYANIDE2WTB3V159FACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
CROTALUS DURISSUS TERRIFICUS VENOM2XF6I0446GACTIB
TOBACCO LEAF6YR2608RSUACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
SPIGELIA ANTHELMIAWYT05213GEACTIB

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-67AMMONIUM CARBONATE, HYDROGEN CYANIDE, CAMPHOR (NATURAL), ACTIVATED CHARCOAL, CROTALUS DURISSUS TERRIFICUS VENOM, TOBACCO LEAF, VERATRUM ALBUM ROOT, AND SPIGELIA ANTHELMIADNA Labs, Inc.202cdebf-12a1-485a-9bd6-05f5eb745dbf2025-01-13WarningsExact identifier
ndc (package): 58264-0067-1
ndc (product): 58264-0067
ndc11 (package): 58264006701
spl id: 2b9ec3c9-bdf0-dcf4-e063-6394a90a24ff
spl set id: 202cdebf-12a1-485a-9bd6-05f5eb745dbf

Reported adverse events (FAERS/openFDA)#

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