BERBERIS VULGARIS 6X liquid

Berberis Vulgaris 6X by

Drug Labeling and Warnings

Berberis Vulgaris 6X by is a Homeopathic medication manufactured, distributed, or labeled by True Botanica, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Berberis vulgaris fruct. 6X

PURPOSE

For temporary relief of radiating body pains, swollen tonsils/adenoids. May also be used for standard homeopathic indications or as directed by your physician.

Use:

For temporary relief of radiating body pains, swollen tonsils/adenoids. May also be used for standard homeopathic indications or as directed by your physician.

Warnings:

Consult your health care provider if symptoms persist more than 5 days or worsen.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

DO NOT USE

TAMPER EVIDENT: Do not use if safety seal is broken before first use.

Directions for Use:

Place drops under tongue for 30 seconds. Adults 7 drops 3 times a day. Children 2-12 years, 7 drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

Other Ingredients:

Citric Acid, Potassium Sorbate, Water

QUESTIONS

Developed and Made by

True Botanica, LLC

1005 Richards Rd., Suite D

Hartland, WI 53029

800-315-8783

www.truebotanica.com

Principal Display Panel

INGREDIENTS AND APPEARANCE

BERBERIS VULGARIS 6X 
berberis vulgaris 6x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53645-1241
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (BERBERIS VULGARIS FRUIT - UNII:6XEF22AHC3)	BERBERIS VULGARIS FRUIT	6 [hp_X]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53645-1241-6	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/22/2024

Labeler - True Botanica, LLC (182071519)

Establishment
Name	Address	ID/FEI	Business Operations
True Botanica, LLC		182071519	manufacture(53645-1241)