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 |