| 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 |