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EB302 ARTHRITIS RELIEF
EB302 ARTHRITIS RELIEF - 53304-0302-1 - (MENTHOL)
Drug Information of EB302 ARTHRITIS RELIEF
| Product NDC: | 53304-0302 |
| Proprietary Name: | EB302 ARTHRITIS RELIEF |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 865.4 mg/50mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EB302 ARTHRITIS RELIEF
| Product NDC: | 53304-0302 |
| Labeler Name: | EMINENCE BIOTECH CORPORATION LIMITED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121101 |
Package Information of EB302 ARTHRITIS RELIEF
| Package NDC: | 53304-0302-1 |
| Package Description: | 1 BOTTLE, SPRAY in 1 BOX (53304-0302-1) > 50 mL in 1 BOTTLE, SPRAY |
NDC Information of EB302 ARTHRITIS RELIEF
| NDC Code | 53304-0302-1 |
| Proprietary Name | EB302 ARTHRITIS RELIEF |
| Package Description | 1 BOTTLE, SPRAY in 1 BOX (53304-0302-1) > 50 mL in 1 BOTTLE, SPRAY |
| Product NDC | 53304-0302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20121101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | EMINENCE BIOTECH CORPORATION LIMITED |
| Substance Name | MENTHOL |
| Strength Number | 865.4 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes |
