FDA.reportPublic FDA data

D-139

Manufacturer
DNA Labs, Inc.
Effective date
2022-06-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:00:06

Label at a glance#

ProductD-139
Active ingredientARSENIC TRIOXIDE, ATROPA BELLADONNA, ACTIVATED CHARCOAL, FERROSOFERRIC PHOSPHATE, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, ANEMONE PRATENSIS
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0147-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Heartburn, acid reflux.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Arsenicum album 6x, 12x, 30x, Belladonna 6x, 12x, 30x, Carbo vegetabilis 6x, 12x, 30x, Ferrum phosphoricum 6x, 12x, 30x, Hydrastis 3x, 6x, 30x, Lycopodium 6x, 12x, 30x, Natrum phosphoricum 6x, 12x, 30x, Nux vomica 6x, 12x, 30x, Phosphorus 6x, 12x, 30x, Pulsatilla 6x, 12x, 30x

INACTIVE

INACTIVE INGREDIENT SECTION

Glycerin, 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 139

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
58264-0147-12022-06-06C16284748780-19d75b9d0-bacd-f424-e053-dadaa90a57ceD-139
58264-0147-12020-01-31C16284748780-19d75b9d0-bacd-f424-e053-dadaa90a57ceD-139

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-014758264-0147-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARSENIC TRIOXIDES7V92P67HOACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
GOLDENSEALZW3Z11D0JVACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PHOSPHORUS27YLU75U4WACTIB
ANEMONE PRATENSIS8E272251DIACTIB

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
2bc3d817-5131-bd62-e063-6394a90a0a5dea7a1270-e540-4933-a1a6-bf93df9549cb2025-01-15WarningsExact identifier
spl set id: ea7a1270-e540-4933-a1a6-bf93df9549cb

Reported adverse events (FAERS/openFDA)#

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