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 |