Berberis Vulgaris

Manufacturer: Warsan Homeopathic
Effective date: 2020-11-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:33:31

Label at a glance#

ProductBerberis Vulgaris

Active ingredientBERBERIS VULGARIS ROOT BARK

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Berberis Vulgaris 30C

INACTIVE INGREDIENT SECTION

Alcohol

Purified Water

WARNINGS SECTION

Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

Do not use if tamper evident seal is missing or broken.

INDICATIONS & USAGE SECTION

Temporary relief from joint pain, itching

OTC - PURPOSE SECTION

Temporary relief from joint pain, itching

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Four drops of water in teaspoon of water 3 times a day as needed.

Children under 12 years of age: Consult doctor prior to use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

berberis vulgaris.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79718-1022-3	2022-01-28	C162847	48780-1	d6a99b39-cca2-a426-e053-dadaa90af4c2	b3c82dff-8aca-6257-e053-2995a90a9f23

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79718-1022-3	Berberis Vulgaris	15 mL in 1 BOTTLE	LIQUID	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79718-1022	BERBERIS VULGARIS LIQUID [WARSAN HOMEOPATHIC]	1	Legacy NDC, 1 package rows	20201113_b3c82dff-8aca-6257-e053-2995a90a9f23.zip

Products#

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

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

Berberis Vulgaris
ALCOHOL
BERBERIS VULGARIS ROOT BARK
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79718-1022	79718-1022-3
79769-1022

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
ALCOHOL	3K9958V90M	IACT
BERBERIS VULGARIS ROOT BARK	1TH8Q20J0U	ACTIB
WATER	059QF0KO0R	IACT

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
b3c82824-c22b-3bda-e053-2995a90a1019			b3c82dff-8aca-6257-e053-2995a90a9f23	2020-11-10	Warnings	Exact identifier spl id: b3c82824-c22b-3bda-e053-2995a90a1019 spl set id: b3c82dff-8aca-6257-e053-2995a90a9f23

Reported adverse events (FAERS/openFDA)#

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