Product NDC: | 51141-0236 |
Proprietary Name: | ATOPALM Oral Pain Relief |
Non Proprietary Name: | BENZOCAINE |
Active Ingredient(s): | 10 g/100g & nbsp; BENZOCAINE |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51141-0236 |
Labeler Name: | NeoPharm, USA |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120206 |
Package NDC: | 51141-0236-7 |
Package Description: | 1 TUBE in 1 BOX (51141-0236-7) > 7 g in 1 TUBE |
NDC Code | 51141-0236-7 |
Proprietary Name | ATOPALM Oral Pain Relief |
Package Description | 1 TUBE in 1 BOX (51141-0236-7) > 7 g in 1 TUBE |
Product NDC | 51141-0236 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOCAINE |
Dosage Form Name | GEL |
Route Name | ORAL |
Start Marketing Date | 20120206 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | NeoPharm, USA |
Substance Name | BENZOCAINE |
Strength Number | 10 |
Strength Unit | g/100g |
Pharmaceutical Classes |