EUPATORIUM PERFOLIATUM

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:48:54

Label at a glance#

ProductEUPATORIUM PERFOLIATUM
Active ingredientEUPATORIUM PERFOLIATUM FLOWERING TOP
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

EUPATORIUM PERFOLIATUM 30K GR

EUPATORIUM PERFOLIATUM 5CH GR

OTC - PURPOSE SECTION

Indications

For the temporary relief of flu symptoms, stiffness,
and aching bones

WARNINGS SECTION

Warning:
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Lactose,
sucrose.

OTC - QUESTIONS SECTION

QUESTIONS? 1-888-737-6925.

DOSAGE & ADMINISTRATION SECTION

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

INDICATIONS & USAGE SECTION

Indications

For the temporary relief of flu symptoms, stiffness and aching bones

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-800062106-8000

UNDA
Do not use if label perforation is broken
Homeopathic Remedy
NDC : 62106-8000-4
EUPATORIUM PERFOLIATUM
Boneset
140 granules
Indications

For the temporary relief of flu symptoms, stiffness,
and aching bones

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
62106-800062106-8000-4

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
0670f957-5579-b040-e063-6394a90a3f532f0cc7a6-2d8d-5dd5-e054-00144ff8d46c2023-09-28WarningsExact identifier
spl set id: 2f0cc7a6-2d8d-5dd5-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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