FDA.reportPublic FDA data

Cocculus indicus

Manufacturer
Washington Homeopathic Products
Effective date
2023-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:22:41

Label at a glance#

ProductCocculus indicus
Active ingredientANAMIRTA COCCULUS SEED
Label structure8 sections

Indications and uses

To relieve the symptoms of motion sickness.

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

COCCULUS

USES

OTC - PURPOSE SECTION

To relieve the symptoms of motion sickness.

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:

COCCULUS   Motion sickness

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 COCCULUS is 4x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Cocculus2023Cocculus2023

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
68428-329-032025-01-30C16284748780-12cef2736-9e1d-d83d-e063-dadaa90ab31fDRUG FACTS
68428-329-052025-01-30C16284748780-12cef2736-9e1d-d83d-e063-dadaa90ab31fDRUG FACTS
68428-329-062025-01-30C16284748780-12cef2736-9e1d-d83d-e063-dadaa90ab31fDRUG FACTS
68428-329-112025-01-30C16284748780-12cef2736-9e1d-d83d-e063-dadaa90ab31fDRUG FACTS
68428-329-122025-01-30C16284748780-12cef2736-9e1d-d83d-e063-dadaa90ab31fDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-329-03Cocculus indicus75 in 1 VIAL, GLASSPELLET753
68428-329-05Cocculus indicus150 in 1 VIAL, GLASSPELLET1503
68428-329-06Cocculus indicus1200 in 1 BOTTLE, GLASSPELLET12003
68428-329-11Cocculus indicus300 in 1 BOTTLE, GLASSPELLET3003
68428-329-12Cocculus indicus600 in 1 BOTTLE, GLASSPELLET6003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-329COCCULUS INDICUS (ANAMIRTA COCCULUS SEED) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]3Legacy NDC, 5 package rows20231019_6e805cc8-3d5b-45d7-ad63-5c72f77d7625.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
68428-32968428-329-03, 68428-329-05, 68428-329-11, 68428-329-12, 68428-329-06

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
ANAMIRTA COCCULUS SEED810258W28UACTIB

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
0803b71c-ea8f-8f79-e063-6294a90a5b516e805cc8-3d5b-45d7-ad63-5c72f77d76252023-10-18WarningsExact identifier
spl id: 0803b71c-ea8f-8f79-e063-6294a90a5b51
spl set id: 6e805cc8-3d5b-45d7-ad63-5c72f77d7625

Reported adverse events (FAERS/openFDA)#

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