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CVS Triple-Thick Antibacterial
CVS Triple-Thick Antibacterial - 59779-005-76 - (Benzalkonium Chloride)
Drug Information of CVS Triple-Thick Antibacterial
| Product NDC: | 59779-005 |
| Proprietary Name: | CVS Triple-Thick Antibacterial |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .12 g/100mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CLOTH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CVS Triple-Thick Antibacterial
| Product NDC: | 59779-005 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111101 |
Package Information of CVS Triple-Thick Antibacterial
| Package NDC: | 59779-005-76 |
| Package Description: | 8 APPLICATOR in 1 PACKAGE (59779-005-76) > 21 mL in 1 APPLICATOR |
NDC Information of CVS Triple-Thick Antibacterial
| NDC Code | 59779-005-76 |
| Proprietary Name | CVS Triple-Thick Antibacterial |
| Package Description | 8 APPLICATOR in 1 PACKAGE (59779-005-76) > 21 mL in 1 APPLICATOR |
| Product NDC | 59779-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | CLOTH |
| Route Name | TOPICAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .12 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
