FDA.reportPublic FDA data

Ignatia amara

Manufacturer
Washington Homeopathic Products
Effective date
2023-10-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:22:48

Label at a glance#

ProductIgnatia amara
Active ingredientSTRYCHNOS IGNATII SEED
Label structure8 sections

Indications and uses

To relieve the symptoms of sadness.

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

IGNATIA

USES

OTC - PURPOSE SECTION

To relieve the symptoms of sadness.

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:

IGNATIA   Sadness

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

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of IGNATIA is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Ignatia2023Ignatia2023

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
68428-435-032025-01-30C16284748780-12cef2736-6570-d83d-e063-dadaa90ab31fDRUG FACTS
68428-435-052025-01-30C16284748780-12cef2736-6570-d83d-e063-dadaa90ab31fDRUG FACTS
68428-435-062025-01-30C16284748780-12cef2736-6570-d83d-e063-dadaa90ab31fDRUG FACTS
68428-435-112025-01-30C16284748780-12cef2736-6570-d83d-e063-dadaa90ab31fDRUG FACTS
68428-435-122025-01-30C16284748780-12cef2736-6570-d83d-e063-dadaa90ab31fDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-435-03Ignatia amara75 in 1 VIAL, GLASSPELLET753
68428-435-05Ignatia amara150 in 1 VIAL, GLASSPELLET1503
68428-435-06Ignatia amara1200 in 1 BOTTLE, GLASSPELLET12003
68428-435-11Ignatia amara300 in 1 BOTTLE, GLASSPELLET3003
68428-435-12Ignatia amara600 in 1 BOTTLE, GLASSPELLET6003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-435IGNATIA AMARA (STRYCHNOS IGNATII SEED) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]3Legacy NDC, 5 package rows20231020_ba9928b1-1895-445b-81d8-c6e190da5d61.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
68428-43568428-435-03, 68428-435-05, 68428-435-11, 68428-435-12, 68428-435-06

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
LACTOSEJ2B2A4N98GIACT
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
SUCROSEC151H8M554IACT

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
0812710b-8eb5-36eb-e063-6394a90a74d2ba9928b1-1895-445b-81d8-c6e190da5d612023-10-19WarningsExact identifier
spl id: 0812710b-8eb5-36eb-e063-6394a90a74d2
spl set id: ba9928b1-1895-445b-81d8-c6e190da5d61

Reported adverse events (FAERS/openFDA)#

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