FDA.reportPublic FDA data

CHAMOMILLA

Manufacturer
STANDARD HOMEOPATHIC COMPANY
Effective date
2018-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:38:31

Label at a glance#

ProductCHAMOMILLA
Active ingredientMATRICARIA CHAMOMILLA
Label structure8 sections

Dosage and administration

Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.

Warnings

WARNINGS SECTION

Do not use if cap band is missing or broken.

If you are pregnant or nursing, consult a licensed health care professional before using this product.

If symptoms persist for 7 days or worsen, contact a licensed practitioner.

To be used according to label indications and/or standard homeopathic indications

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of the reach of children

OTC - QUESTIONS SECTION

Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional

INACTIVE INGREDIENT SECTION

In a base of Acacia Gum and Lactose N.F

OTC - ACTIVE INGREDIENT SECTION

CHAMOMILLA 30X

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

OCCASIONAL SLEEPLESSNESS, IRRITABILITY

Principal Display Panel -- 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0119-01

Homeopathic Medicine

CHAMOMILLA

30X

OCCASIONAL

SLEEPLESSNESS,

IRRITABILITY*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

labellabel

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
0360-01190360-0119-01

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
ACACIA5C5403N26OIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
MATRICARIA CHAMOMILLAG0R4UBI2ZZACTIB

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
fd7c79ee-e2d9-ff7e-e053-6294a90a1e7b4be4f8fa-704b-57fc-e054-00144ff8d46c2023-06-06WarningsExact identifier
spl set id: 4be4f8fa-704b-57fc-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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