Product NDC: | 67510-0058 |
Proprietary Name: | Oral Pain Relief |
Non Proprietary Name: | Oral Pain Reliever |
Active Ingredient(s): | 200 mg/g & nbsp; Oral Pain Reliever |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67510-0058 |
Labeler Name: | Kareway Product, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110717 |
Package NDC: | 67510-0058-4 |
Package Description: | 1 TUBE in 1 CARTON (67510-0058-4) > 11.9 g in 1 TUBE |
NDC Code | 67510-0058-4 |
Proprietary Name | Oral Pain Relief |
Package Description | 1 TUBE in 1 CARTON (67510-0058-4) > 11.9 g in 1 TUBE |
Product NDC | 67510-0058 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Oral Pain Reliever |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110717 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Kareway Product, Inc. |
Substance Name | BENZOCAINE |
Strength Number | 200 |
Strength Unit | mg/g |
Pharmaceutical Classes |