Product NDC: | 14060-002 |
Proprietary Name: | BeeGentle |
Non Proprietary Name: | benzocaine |
Active Ingredient(s): | 210 mg/g & nbsp; benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14060-002 |
Labeler Name: | CAO Group, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100901 |
Package NDC: | 14060-002-03 |
Package Description: | 3 SYRINGE, PLASTIC in 1 KIT (14060-002-03) > 3 g in 1 SYRINGE, PLASTIC |
NDC Code | 14060-002-03 |
Proprietary Name | BeeGentle |
Package Description | 3 SYRINGE, PLASTIC in 1 KIT (14060-002-03) > 3 g in 1 SYRINGE, PLASTIC |
Product NDC | 14060-002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | benzocaine |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100901 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | CAO Group, Inc. |
Substance Name | BENZOCAINE |
Strength Number | 210 |
Strength Unit | mg/g |
Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |