BERBERIS VULGARIS liquid

Berberis Vulgaris by

Drug Labeling and Warnings

Berberis Vulgaris by is a Homeopathic medication manufactured, distributed, or labeled by Warsan Homeopathic. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Berberis Vulgaris 30C

INACTIVE INGREDIENT

Alcohol

Purified Water

WARNINGS

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

Temporary relief from joint pain, itching

PURPOSE

Temporary relief from joint pain, itching

DOSAGE & ADMINISTRATION

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BERBERIS VULGARIS 
berberis vulgaris liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79718-1022(NDC:79769-1022)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	30 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79718-1022-3	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/13/2020

Labeler - Warsan Homeopathic (081031642)