Product NDC: | 10157-9302 |
Proprietary Name: | Blistex |
Non Proprietary Name: | Benzocaine and Chloroxylenol |
Active Ingredient(s): | 5; .1 g/100g; g/100g & nbsp; Benzocaine and Chloroxylenol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10157-9302 |
Labeler Name: | Blistex Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130305 |
Package NDC: | 10157-9302-4 |
Package Description: | 1 TUBE in 1 CARTON (10157-9302-4) > 28 g in 1 TUBE |
NDC Code | 10157-9302-4 |
Proprietary Name | Blistex |
Package Description | 1 TUBE in 1 CARTON (10157-9302-4) > 28 g in 1 TUBE |
Product NDC | 10157-9302 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine and Chloroxylenol |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20130305 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Blistex Inc. |
Substance Name | BENZOCAINE; CHLOROXYLENOL |
Strength Number | 5; .1 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |