| Product NDC: | 41250-701 |
| Proprietary Name: | Oral Analgesic |
| 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: | 41250-701 |
| Labeler Name: | Meijer Distribution, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100513 |
| Package NDC: | 41250-701-25 |
| Package Description: | 1 TUBE in 1 CARTON (41250-701-25) > 7.1 g in 1 TUBE |
| NDC Code | 41250-701-25 |
| Proprietary Name | Oral Analgesic |
| Package Description | 1 TUBE in 1 CARTON (41250-701-25) > 7.1 g in 1 TUBE |
| Product NDC | 41250-701 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oral Pain Reliever |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100513 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Meijer Distribution, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |