Product NDC: | 63044-030 |
Proprietary Name: | ZIKS ARTHRITIS PAIN RELIEF |
Non Proprietary Name: | ZIKS ARTHRITIS PAIN RELIEF |
Active Ingredient(s): | .014; .566; 6.79 mg/g; mg/g; mg/g & nbsp; ZIKS ARTHRITIS PAIN RELIEF |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63044-030 |
Labeler Name: | Nnodum Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19991110 |
Package NDC: | 63044-030-60 |
Package Description: | 56.6 g in 1 TUBE (63044-030-60) |
NDC Code | 63044-030-60 |
Proprietary Name | ZIKS ARTHRITIS PAIN RELIEF |
Package Description | 56.6 g in 1 TUBE (63044-030-60) |
Product NDC | 63044-030 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZIKS ARTHRITIS PAIN RELIEF |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19991110 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Nnodum Pharmaceuticals |
Substance Name | CAPSAICIN; MENTHOL; METHYL SALICYLATE |
Strength Number | .014; .566; 6.79 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |