Product NDC: | 50672-838 |
Proprietary Name: | Antibacterial Wet Wipes |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | .1 g/100g & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50672-838 |
Labeler Name: | MC Group Development Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121112 |
Package NDC: | 50672-838-01 |
Package Description: | 3.3 g in 1 POUCH (50672-838-01) |
NDC Code | 50672-838-01 |
Proprietary Name | Antibacterial Wet Wipes |
Package Description | 3.3 g in 1 POUCH (50672-838-01) |
Product NDC | 50672-838 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 20121112 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MC Group Development Ltd. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .1 |
Strength Unit | g/100g |
Pharmaceutical Classes |