Product NDC: | 29500-1000 |
Proprietary Name: | Personal Care |
Non Proprietary Name: | Alcohol, Benzethonium Chloride |
Active Ingredient(s): | & nbsp; Alcohol, Benzethonium Chloride |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29500-1000 |
Labeler Name: | Personal Care Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091101 |
Package NDC: | 29500-1000-4 |
Package Description: | 1 KIT in 1 KIT (29500-1000-4) * 60 mL in 1 BOTTLE (29500-9085-1) * 1 SWAB in 1 PACKET (29500-9084-2) |
NDC Code | 29500-1000-4 |
Proprietary Name | Personal Care |
Package Description | 1 KIT in 1 KIT (29500-1000-4) * 60 mL in 1 BOTTLE (29500-9085-1) * 1 SWAB in 1 PACKET (29500-9084-2) |
Product NDC | 29500-1000 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol, Benzethonium Chloride |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20091101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Personal Care Products, Inc. |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |