DULCAMARA

Manufacturer: STANDARD HOMEOPATHIC COMPANY
Effective date: 2021-11-09
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:28:38

Label at a glance#

ProductDULCAMARA

Active ingredientSOLANUM DULCAMARA TOP

Label structure8 sections

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact800-624-9659

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

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

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Do not use if cap band is missing or broken.

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of the reach of children.

SPL UNCLASSIFIED SECTION

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

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

DULCAMARA 30X

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

COUGH OR MINOR RHEUMATIC PAIN

Principal Display Panel -- 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0159-01

Homeopathic Medicine

DULCAMARA

30X

COUGH OR MINOR

RHEUMATIC PAIN*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated

250 TABLETS

label

Products#

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

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

DULCAMARA
ACACIA
LACTOSE MONOHYDRATE
SOLANUM DULCAMARA TOP

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0360-0159	0360-0159-01

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
Name	UNII	Kind
ACACIA	5C5403N26O	IACT
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
SOLANUM DULCAMARA TOP	KPS1B1162N	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d0604720-623c-e8a9-e053-2995a90ab0e6			4c6d6ec3-a3fb-670c-e054-00144ff88e88	2021-11-09	Warnings	Exact identifier spl id: d0604720-623c-e8a9-e053-2995a90ab0e6 spl set id: 4c6d6ec3-a3fb-670c-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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