FDA.reportPublic FDA data

Bestmade Natural Products Berberis Vulgaris

Manufacturer
Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date
2025-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:59

Label at a glance#

ProductBestmade Natural Products Berberis Vulgaris
Active ingredientBERBERIS VULGARIS ROOT BARK
Label structure8 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Alcohol base to preserve product.

INDICATIONS & USAGE SECTION

Use: Temporarily relieves discomfort and pain in the kidney area and colic-like discomfort; scalp tightness, urinary irritation, itching, skin pigmentation, and nausea before breakfast.*

OTC - PURPOSE SECTION

Use: Temporarily relieves discomfort and pain in the kidney area and colic-like discomfort; scalp tightness, urinary irritation, itching, skin pigmentation, and nausea before breakfast.*

DOSAGE & ADMINISTRATION SECTION

Dosage Instructions: 10 drops in a spoon of water 3 times a day. For people under 100lb: use half a dose or take as prescribed.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Berberis Vulgaris Ø (HPUS)

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.

*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.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire Package Label

Berberis VulgBerberis Vulg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82969-5121-1Bestmade Natural Products Berberis Vulgaris30 mL in 1 BOTTLE, GLASSTINCTURE301

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
82969-512182969-5121-1

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
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

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 Berberis VulgarisBERBERIS VULGARISBestmade Natural Products36d330ab-7656-0bf3-e063-6294a90af7ab2025-06-05WarningsExact identifier
ndc (package): 82969-5121-1
ndc (product): 82969-5121
ndc11 (package): 82969512101
spl id: 36d330ab-7657-0bf3-e063-6294a90af7ab
spl set id: 36d330ab-7656-0bf3-e063-6294a90af7ab

Reported adverse events (FAERS/openFDA)#

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