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 |