Bestmade Natural Products Eupatorium Perf

Manufacturer
Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date
2025-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:18

Label at a glance#

ProductBestmade Natural Products Eupatorium Perf
Active ingredientEUPATORIUM PERFOLIATUM FLOWERING TOP
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

How to Use

Take with water 3-4 times a day. Ages 12 or older, 5 Pellets, Ages 12-2, 3 Pellets, Ages below 2, consult your Doctor.

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves occasional aches in limbs and muscles that accompany elevated body temperature, chills, and discomfort.*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

OTC - PURPOSE SECTION

Uses

Temporarily relieves occasional aches in limbs and muscles that accompany elevated body temperature, chills, and discomfort.*

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

INACTIVE INGREDIENT SECTION

Ingredients

Inactive: Sucrose/Lactose Pellets base to Preserve Remedy

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Eupatorium Perfoliatum (Common Boneset [HPUS] 30c potency

WARNINGS SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

This product is not intended to diagnose, treat, cure, or prevent any disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire package label

eupatorium perfeupatorium perf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82969-5051-1Bestmade Natural Products Eupatorium Perf30 [hp_C] in 1 BOTTLE, GLASSTABLET, SOLUBLE301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82969-5051BESTMADE NATURAL PRODUCTS EUPATORIUM PERF (EUPATORIUM PERFOLIATUM) TABLET, SOLUBLE [BESTMADE NATURAL PRODUCTS]1Current NDC, 1 package rows20250308_2f983421-5006-58f0-e063-6294a90a440d.zip

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
82969-505182969-5051-1

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
Bestmade Natural Products Eupatorium PerfEUPATORIUM PERFOLIATUMBestmade Natural Products2f983421-5006-58f0-e063-6294a90a440d2025-03-05WarningsExact identifier
ndc (package): 82969-5051-1
ndc (product): 82969-5051
ndc11 (package): 82969505101
spl id: 2f983421-5007-58f0-e063-6294a90a440d
spl set id: 2f983421-5006-58f0-e063-6294a90a440d

Reported adverse events (FAERS/openFDA)#

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