| Product NDC: | 0363-6230 |
| Proprietary Name: | Walgreens |
| 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: | 0363-6230 |
| Labeler Name: | Walgreens |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110120 |
| Package NDC: | 0363-6230-09 |
| Package Description: | 1 TUBE in 1 CARTON (0363-6230-09) > 14 g in 1 TUBE (0363-6230-02) |
| NDC Code | 0363-6230-09 |
| Proprietary Name | Walgreens |
| Package Description | 1 TUBE in 1 CARTON (0363-6230-09) > 14 g in 1 TUBE (0363-6230-02) |
| Product NDC | 0363-6230 |
| 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 | Walgreens |
| Substance Name | BENZOCAINE |
| Strength Number | 7.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |