FDA.reportPublic FDA data

Eschscholtzia californica

Manufacturer
Washington Homeopathic Products
Effective date
2020-12-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:58:36

Label at a glance#

ProductEschscholtzia californica
Active ingredientESCHSCHOLZIA CALIFORNICA
Label structure9 sections

Indications and uses

To relieve the symptoms of sleeplessness.

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

ESCHSCHOLTZIA

USES

OTC - PURPOSE SECTION

To relieve the symptoms of sleeplessness.

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:

ESCHSCHOLTZIA Sleeplessness

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

Changes

RECENT MAJOR CHANGES SECTION

Indications

Indications:

ESCHSCHOLTZIA Wheezing

--Changes to --

Indications:

ESCHSCHOLTZIA Sleeplessness

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of ESCHSCHOLTZIA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.
LabelLabel
Availability is subject to change.

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.

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
68428-37268428-372-03, 68428-372-05, 68428-372-11, 68428-372-12, 68428-372-06

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
ESCHSCHOLZIA CALIFORNICA9315HN272XACTIB

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
db86b887-39a6-0e6d-e053-2995a90a5cbf63e4c48b-4895-45c9-a4e5-10aa474699922022-03-31WarningsExact identifier
spl set id: 63e4c48b-4895-45c9-a4e5-10aa47469992

Reported adverse events (FAERS/openFDA)#

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