| 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 |