| Product NDC: | 11822-0317 |
| Proprietary Name: | Rite Aid |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | .04; 20; .1 g/100g; g/100g; g/100g & nbsp; Benzocaine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-0317 |
| Labeler Name: | Rite Aid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110120 |
| Package NDC: | 11822-0317-9 |
| Package Description: | 1 TUBE in 1 CARTON (11822-0317-9) > 11.9 g in 1 TUBE (11822-0317-2) |
| NDC Code | 11822-0317-9 |
| Proprietary Name | Rite Aid |
| Package Description | 1 TUBE in 1 CARTON (11822-0317-9) > 11.9 g in 1 TUBE (11822-0317-2) |
| Product NDC | 11822-0317 |
| 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 NOT FINAL |
| Labeler Name | Rite Aid |
| Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE; ZINC CHLORIDE |
| Strength Number | .04; 20; .1 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |