| Product NDC: | 63868-953 |
| Proprietary Name: | Quality Choice Maximum Strength Oral Pain Relieving |
| Non Proprietary Name: | BENZOCAINE |
| Active Ingredient(s): | 20 g/100g & nbsp; BENZOCAINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63868-953 |
| Labeler Name: | Chain Drug Marketing Association Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130531 |
| Package NDC: | 63868-953-11 |
| Package Description: | 1 TUBE in 1 CARTON (63868-953-11) > 11.76 g in 1 TUBE |
| NDC Code | 63868-953-11 |
| Proprietary Name | Quality Choice Maximum Strength Oral Pain Relieving |
| Package Description | 1 TUBE in 1 CARTON (63868-953-11) > 11.76 g in 1 TUBE |
| Product NDC | 63868-953 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOCAINE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130531 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Chain Drug Marketing Association Inc |
| Substance Name | BENZOCAINE |
| Strength Number | 20 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |