| Product NDC: | 00904-5899 |
| Proprietary Name: | Major Oral Pain Relief |
| Non Proprietary Name: | Oral Anesthetic |
| Active Ingredient(s): | 200 mg/mL & nbsp; Oral Anesthetic |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 00904-5899 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080801 |
| Package NDC: | 00904-5899-4 |
| Package Description: | 1 BOTTLE, GLASS in 1 BLISTER PACK (00904-5899-4) > 15 mL in 1 BOTTLE, GLASS (00904-5899-3) |
| NDC Code | 00904-5899-4 |
| Proprietary Name | Major Oral Pain Relief |
| Package Description | 1 BOTTLE, GLASS in 1 BLISTER PACK (00904-5899-4) > 15 mL in 1 BOTTLE, GLASS (00904-5899-3) |
| Product NDC | 00904-5899 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oral Anesthetic |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |