BERBERIS ANTISEPTIC- berberis aquifolium, calendula officinalis, hydrastis canadensis, acid boric, zinc oxide, borax, calcium sulphate, antimonium crudum cream

Berberis by

Drug Labeling and Warnings

Berberis by is a Homeopathic medication manufactured, distributed, or labeled by Curative Power Lab PVT LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Berberis Aq. - 0.1ml
Calendula - 0.1ml
Hydrastis Can. - 0.1ml
Acid Boric - 1x 10mg
Zinc Oxide - 1x 5mg
Borax - 1x5mg
Calc. Sulph. - 1x 2mg
Ant. Crude - 1x 2mg

INACTIVE INGREDIENT

Alcohol - 4.8 percent v/v

PURPOSE

Berberis is a flowered shrub known to aid in the care of acne, blemishes, and the smoothing of complexion. The unique combination of Berberis Antiseptic Cream helps to cleanse pores and leaves your skin feeling silky smooth.

INDICATIONS & USAGE

Berberis. A natural solution for acne and blemishes.

- Cleanses Pores

-Clears Complexion

DOSAGE & ADMINISTRATION

Apply and rub onto skin as needed.

WARNINGS

- For external use only.

- Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

HOW SUPPLIED

Berberis Antiseptic Cream is manufactured in India with the highest quality ingredients for Regranion, LLC, Charleston, SC 29403

REFERENCES

Questions? Comments?
Call 1-877-648-8443

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BERBERIS  ANTISEPTIC
berberis aquifolium, calendula officinalis, hydrastis canadensis, acid boric, zinc oxide, borax, calcium sulphate, antimonium crudum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51720-421
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (MAHONIA AQUIFOLIUM ROOT BARK - UNII:VZJ9F3C3SB)	MAHONIA AQUIFOLIUM ROOT BARK	2 [hp_X]  in 21 g
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ)	CALENDULA OFFICINALIS FLOWERING TOP	2 [hp_X]  in 21 g
GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV)	GOLDENSEAL	2 [hp_X]  in 21 g
BORIC ACID (UNII: R57ZHV85D4) (BORIC ACID - UNII:R57ZHV85D4)	BORIC ACID	1 [hp_X]  in 21 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1 [hp_X]  in 21 g
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	1 [hp_X]  in 21 g
CALCIUM SULFATE (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE	1 [hp_X]  in 21 g
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY - UNII:9IT35J3UV3)	ANTIMONY TRISULFIDE	1 [hp_X]  in 21 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)	1 mL  in 21 g

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51720-421-58	1 in 1 BOX
1	NDC: 51720-421-56	21 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/2009

Labeler - Curative Power Lab PVT LTD (650500981)

Registrant - Curative Power Lab PVT LTD (650500981)

Establishment
Name	Address	ID/FEI	Business Operations
Curative Power Lab PVT LTD		650500981	manufacture