Berberis Antiseptic is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Curative Power Lab Pvt Ltd. The primary component is Mahonia Aquifolium Root Bark; Calendula Officinalis Flowering Top; Goldenseal; Boric Acid; Zinc Oxide; Sodium Borate; Calcium Sulfate; Antimony Trisulfide.
Product ID | 51720-421_817bad9e-3bc0-44bd-b626-e1c6def461fb |
NDC | 51720-421 |
Product Type | Human Otc Drug |
Proprietary Name | Berberis Antiseptic |
Generic Name | Berberis Aquifolium, Calendula Officinalis, Hydrastis Canadensis, Acid Boric, Zinc Oxide, Borax, Calcium Sulphate, Antimonium Crudum |
Dosage Form | Cream |
Route of Administration | TOPICAL |
Marketing Start Date | 2009-08-15 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Curative Power Lab PVT LTD |
Substance Name | MAHONIA AQUIFOLIUM ROOT BARK; CALENDULA OFFICINALIS FLOWERING TOP; GOLDENSEAL; BORIC ACID; ZINC OXIDE; SODIUM BORATE; CALCIUM SULFATE; ANTIMONY TRISULFIDE |
Active Ingredient Strength | 2 [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2009-08-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-08-15 |
Inactivation Date | 2019-10-29 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-08-15 |
Ingredient | Strength |
---|---|
MAHONIA AQUIFOLIUM ROOT BARK | 2 [hp_X]/21g |
SPL SET ID: | 157d1a6c-9596-4118-9792-f195edd6d90f |
Manufacturer | |
UNII | |
UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BERBERIS 79283847 not registered Live/Pending |
PLASTIA s.r.o. 2019-10-16 |