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 |