SANGUINARIA CAN

Manufacturer
Standard Homeopathic Company
Effective date
2018-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:52:01

Label at a glance#

ProductSANGUINARIA CAN
Active ingredientSANGUINARIA CANADENSIS ROOT
Label structure9 sections

Dosage and administration

Adults: Disolve 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

OTC - DO NOT USE SECTION

Do not use if cap band is missing or broken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or nursing,

consult a licensed beforeusing this product.

OTC - ASK DOCTOR 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.

SPL UNCLASSIFIED SECTION

Standard Homeopathic Company

Los Angeles, CA 90061

Questions?

OTC - QUESTIONS SECTION

800-624-9659

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

SANGUINARIA CAN.

30X

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

HEADACHE, COLD OR FLU*

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Disolve 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.

Principal Display Panel - 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

STANDARD

HOMEOPATHIC

MADE IN THE USA SINCE 1903

NDC # 0360-0396-01

Homeopathic Medicine

SANGUINARIA CAN.

30X

HEADACHE, COLD OR FLU*

*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 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0360-03960360-0396-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
ff4b5190-6b51-4f95-e053-6294a90ab72e758abf53-ad86-62ac-e053-2991aa0a8f0c2023-06-29WarningsExact identifier
spl set id: 758abf53-ad86-62ac-e053-2991aa0a8f0c

Reported adverse events (FAERS/openFDA)#

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