Product NDC: | 11822-3950 |
Proprietary Name: | Rite Aid Liquid Anesthetic Oral Pain Relief |
Non Proprietary Name: | BENZOCAINE |
Active Ingredient(s): | 200 mg/mL & nbsp; BENZOCAINE |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-3950 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100708 |
Package NDC: | 11822-3950-6 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (11822-3950-6) > 30 mL in 1 TUBE, WITH APPLICATOR |
NDC Code | 11822-3950-6 |
Proprietary Name | Rite Aid Liquid Anesthetic Oral Pain Relief |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (11822-3950-6) > 30 mL in 1 TUBE, WITH APPLICATOR |
Product NDC | 11822-3950 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOCAINE |
Dosage Form Name | GEL |
Route Name | ORAL |
Start Marketing Date | 20100708 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rite Aid Corporation |
Substance Name | BENZOCAINE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes |