FDA.reportPublic FDA data

BM Digitalis Purpurea

Manufacturer
BM Private Limited
Effective date
2026-09-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-29 01:02:19

Label at a glance#

ProductBM Digitalis Purpurea
Active ingredientDIGITALIS
Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Indications & dosage:
Referred to enclosed self help guide or as advised by a homoeopathic physician.

INACTIVE INGREDIENT SECTION

sucrose

OTC - ACTIVE INGREDIENT SECTION

Digitalis Purpurea

INDICATIONS & USAGE SECTION

Indications & dosage:
Referred to enclosed self help guide or as advised by a homoeopathic physician.

OTC - PURPOSE SECTION

Indications & dosage:
Referred to enclosed self help guide or as advised by a homoeopathic physician.

CONTRAINDICATIONS SECTION

Care & contra-indications:
This is a homoeopathic remedy, no contra-indications are established.

WARNINGS SECTION

Precautions/storage:
Keep away from children and store at cool and dry place.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Precautions/storage:
Keep away from children and store at cool and dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Digitalis purpurea 30.jpgDigitalis purpurea 30.jpgEntire package

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-510685816-5106-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIGITALISF1T8QT9U8BACTIB
SUCROSEC151H8M554IACT
GELATIN2G86QN327LIACT
MAGNESIUM STEARATE70097M6I30IACT
SILICON DIOXIDEETJ7Z6XBU4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-01full-release2026-06-01 02:34:16

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
BM Digitalis PurpureaDIGITALIS PURPUREABM Private Limited38dfb441-b08a-b6a8-e063-6394a90a72ef2025-07-01WarningsExact identifier
ndc (package): 85816-5106-1
ndc (product): 85816-5106
ndc11 (package): 85816510601
spl set id: 38dfb441-b08a-b6a8-e063-6394a90a72ef

Reported adverse events (FAERS/openFDA)#

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