Product NDC: | 11822-1031 |
Proprietary Name: | Rite Aid |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | 7.5 g/100g & nbsp; Benzocaine |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-1031 |
Labeler Name: | Rite Aid |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110120 |
Package NDC: | 11822-1031-9 |
Package Description: | 1 TUBE in 1 CARTON (11822-1031-9) > 14 g in 1 TUBE (11822-1031-2) |
NDC Code | 11822-1031-9 |
Proprietary Name | Rite Aid |
Package Description | 1 TUBE in 1 CARTON (11822-1031-9) > 14 g in 1 TUBE (11822-1031-2) |
Product NDC | 11822-1031 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | ORAL |
Start Marketing Date | 20110120 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rite Aid |
Substance Name | BENZOCAINE |
Strength Number | 7.5 |
Strength Unit | g/100g |
Pharmaceutical Classes |