BERBERIS AQUIFOLIUM- berberis aquifolium root bark liquid

Berberis aquifolium by

Drug Labeling and Warnings

Berberis aquifolium by is a Homeopathic medication manufactured, distributed, or labeled by Washington Homeopathic Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

BERBERIS AQUI

USES

To relieve the symptoms of acne.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

BERBERIS AQUI   Acne

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

DIRECTIONS

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

The OTC potency range of BERBERIS AQUI is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

INGREDIENTS AND APPEARANCE

BERBERIS AQUIFOLIUM 
berberis aquifolium root bark liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71919-119
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (BERBERIS AQUIFOLIUM ROOT BARK - UNII:VZJ9F3C3SB)	BERBERIS AQUIFOLIUM ROOT BARK	30 [hp_C]  in 1 mL

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

Product Characteristics
Color	white (white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71919-119-07	15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	04/29/2010
2	NDC: 71919-119-08	30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	04/29/2010
3	NDC: 71919-119-09	50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	04/29/2010
4	NDC: 71919-119-10	100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	04/29/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/29/2010

Labeler - Washington Homeopathic Products (084929389)

Establishment
Name	Address	ID/FEI	Business Operations
Washington Homeopathic Products		084929389	manufacture(71919-119)