| Product NDC: | 51720-421 |
| Proprietary Name: | Berberis |
| Non Proprietary Name: | Berberis Aquifolium, Calendula Officinalis, Hydrastis Canadensis, Acid Boric, Zinc Oxide, Borax, Calcium Sulphate, Antimonium Crudum |
| Active Ingredient(s): | 1; 1; 1; 2; 2; 2; 1; 1 [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g & nbsp; Berberis Aquifolium, Calendula Officinalis, Hydrastis Canadensis, Acid Boric, Zinc Oxide, Borax, Calcium Sulphate, Antimonium Crudum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51720-421 |
| Labeler Name: | Curative Power Lab PVT LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090815 |
| Package NDC: | 51720-421-58 |
| Package Description: | 1 TUBE in 1 BOX (51720-421-58) > 21 g in 1 TUBE (51720-421-56) |
| NDC Code | 51720-421-58 |
| Proprietary Name | Berberis |
| Package Description | 1 TUBE in 1 BOX (51720-421-58) > 21 g in 1 TUBE (51720-421-56) |
| Product NDC | 51720-421 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Berberis Aquifolium, Calendula Officinalis, Hydrastis Canadensis, Acid Boric, Zinc Oxide, Borax, Calcium Sulphate, Antimonium Crudum |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090815 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Curative Power Lab PVT LTD |
| Substance Name | ANTIMONY TRISULFIDE; BORIC ACID; CALCIUM SULFATE; CALENDULA OFFICINALIS FLOWERING TOP; GOLDENSEAL; MAHONIA AQUIFOLIUM ROOT BARK; SODIUM BORATE; ZINC OXIDE |
| Strength Number | 1; 1; 1; 2; 2; 2; 1; 1 |
| Strength Unit | [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g; [hp_X]/21g |
| Pharmaceutical Classes |