| Product NDC: | 55312-407 |
| Proprietary Name: | Western Family Cold Sore Treatment |
| Non Proprietary Name: | Camphor |
| Active Ingredient(s): | 1.3; 30 mg/g; mg/g & nbsp; Camphor |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55312-407 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130410 |
| Package NDC: | 55312-407-01 |
| Package Description: | 1 TUBE in 1 PACKAGE (55312-407-01) > 2 g in 1 TUBE |
| NDC Code | 55312-407-01 |
| Proprietary Name | Western Family Cold Sore Treatment |
| Package Description | 1 TUBE in 1 PACKAGE (55312-407-01) > 2 g in 1 TUBE |
| Product NDC | 55312-407 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Camphor |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130410 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Western Family Foods Inc |
| Substance Name | BENZALKONIUM CHLORIDE; CAMPHOR (SYNTHETIC) |
| Strength Number | 1.3; 30 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |