FDA.reportPublic FDA data

Digitalis pupurea

Manufacturer
Washington Homeopathic Products
Effective date
2022-12-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:49

Label at a glance#

ProductDigitalis pupurea
Active ingredientDIGITALIS
Label structure9 sections

Indications and uses

To relieve the symptoms of worry.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

DIGITALIS

USES

OTC - PURPOSE SECTION

To relieve the symptoms of worry.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

DIGITALIS Worry

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

RECENT MAJOR CHANGES SECTION

Indication: Worry

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of DIGITALIS is 4x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Digitalis purpureaDigitalis purpurea

All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68428-357-032025-01-30C16284748780-12cef2736-8770-d83d-e063-dadaa90ab31fDRUG FACTS
68428-357-052025-01-30C16284748780-12cef2736-8770-d83d-e063-dadaa90ab31fDRUG FACTS
68428-357-062025-01-30C16284748780-12cef2736-8770-d83d-e063-dadaa90ab31fDRUG FACTS
68428-357-112025-01-30C16284748780-12cef2736-8770-d83d-e063-dadaa90ab31fDRUG FACTS
68428-357-122025-01-30C16284748780-12cef2736-8770-d83d-e063-dadaa90ab31fDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-357-03Digitalis pupurea75 in 1 VIAL, GLASSPELLET754
68428-357-05Digitalis pupurea150 in 1 VIAL, GLASSPELLET1504
68428-357-06Digitalis pupurea1200 in 1 BOTTLE, GLASSPELLET12004
68428-357-11Digitalis pupurea300 in 1 BOTTLE, GLASSPELLET3004
68428-357-12Digitalis pupurea600 in 1 BOTTLE, GLASSPELLET6004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-357DIGITALIS PUPUREA (DIGITALIS) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]4Legacy NDC, 5 package rows20221209_5b1601ed-aa4a-4ff4-a9d4-2caa5ff1e312.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68428-35768428-357-03, 68428-357-05, 68428-357-11, 68428-357-12, 68428-357-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
DIGITALISF1T8QT9U8BACTIB

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
ef52ae2e-91a6-85d4-e053-2a95a90a117d5b1601ed-aa4a-4ff4-a9d4-2caa5ff1e3122022-12-08WarningsExact identifier
spl id: ef52ae2e-91a6-85d4-e053-2a95a90a117d
spl set id: 5b1601ed-aa4a-4ff4-a9d4-2caa5ff1e312

Reported adverse events (FAERS/openFDA)#

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