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Saniquat Foaming hand sanitizer
Saniquat Foaming hand sanitizer - 16038-001-01 - (Benzalkonium Chloride)
Drug Information of Saniquat Foaming hand sanitizer
| Product NDC: | 16038-001 |
| Proprietary Name: | Saniquat Foaming hand sanitizer |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .1 mL/100mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Saniquat Foaming hand sanitizer
| Product NDC: | 16038-001 |
| Labeler Name: | West Penetone Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100207 |
Package Information of Saniquat Foaming hand sanitizer
| Package NDC: | 16038-001-01 |
| Package Description: | 250 mL in 1 BOTTLE, PUMP (16038-001-01) |
NDC Information of Saniquat Foaming hand sanitizer
| NDC Code | 16038-001-01 |
| Proprietary Name | Saniquat Foaming hand sanitizer |
| Package Description | 250 mL in 1 BOTTLE, PUMP (16038-001-01) |
| Product NDC | 16038-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100207 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | West Penetone Inc |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
