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Cold Sore Treatment
Cold Sore Treatment - 49738-200-41 - (Benzalkonium Chloride)
Drug Information of Cold Sore Treatment
| Product NDC: | 49738-200 |
| Proprietary Name: | Cold Sore Treatment |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .13 mL/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | TINCTURE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Sore Treatment
| Product NDC: | 49738-200 |
| Labeler Name: | Kmart Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of Cold Sore Treatment
| Package NDC: | 49738-200-41 |
| Package Description: | 2 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (49738-200-41) > .6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
NDC Information of Cold Sore Treatment
| NDC Code | 49738-200-41 |
| Proprietary Name | Cold Sore Treatment |
| Package Description | 2 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (49738-200-41) > .6 mL in 1 VIAL, PATENT DELIVERY SYSTEM |
| Product NDC | 49738-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | TINCTURE |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kmart Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
