FDA.reportPublic FDA data

D-139

Manufacturer
DNA Labs, Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:31:25

Label at a glance#

ProductD-139
Active ingredientANEMONE PRATENSIS, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, FERROSOFERRIC PHOSPHATE, ARSENIC TRIIODIDE, ATROPA BELLADONNA, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, ACTIVATED CHARCOAL, OYSTER SHELL CALCIUM CARBONATE, CRUDE, GOLDENSEAL, STRYCHNOS NUX-VOMICA SEED
Label structure8 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0163-1

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Heartburn, acid reflux.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Arsenicum album 6x, Belladonna 6x, Calcarea carbonica 6x, Carbo vegetabilis 6x, Ferrum phosphoricum 6x, Lycopodium 6x, Natrum phosphoricum 6x, Nux vomica 6x, Phosphorus 6x, Pulsatilla 6x, Hydratsis 3x

INACTIVE

INACTIVE INGREDIENT SECTION

20% alcohol in purified water.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper under tongue two times daily. Acute symptoms 1/2 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.

D-139 DIST Label Proof 9.22.jpgD-139 DIST Label Proof 9.22.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0163-1D-13929.57 mL in 1 BOTTLE, GLASSSOLUTION29.572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0163D-139 (ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARBO VEGETABILIS, FERRUM PHOSPHORICUM, LYCOPODIUM, NATRUM PHOSPHORICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA, HYDRASTIS) SOLUTION [DNA LABS, INC.]2Current NDC, Legacy NDC, 1 package rows20250115_e830774e-35c8-7309-e053-2995a90ae043.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58264-016358264-0163-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANEMONE PRATENSIS8E272251DIACTIB
ALCOHOL3K9958V90MIACT
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
PHOSPHORUS27YLU75U4WACTIB
WATER059QF0KO0RIACT
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
ARSENIC TRIIODIDE3029988O2TACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
GOLDENSEALZW3Z11D0JVACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB

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-139ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARBO VEGETABILIS, FERRUM PHOSPHORICUM, LYCOPODIUM, NATRUM PHOSPHORICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA, HYDRASTISDNA Labs, Inc.e830774e-35c8-7309-e053-2995a90ae0432025-01-13WarningsExact identifier
ndc (package): 58264-0163-1
ndc (product): 58264-0163
ndc11 (package): 58264016301
spl id: 2b9f0ae7-5ebc-31e5-e063-6294a90a6ebf
spl set id: e830774e-35c8-7309-e053-2995a90ae043

Reported adverse events (FAERS/openFDA)#

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