| Product NDC: | 0436-0672 |
| Proprietary Name: | Dakins Quarter |
| Non Proprietary Name: | Sodium Hypochlorite |
| Active Ingredient(s): | 1.25 mg/mL & nbsp; Sodium Hypochlorite |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0436-0672 |
| Labeler Name: | Century Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060524 |
| Package NDC: | 0436-0672-16 |
| Package Description: | 473 mL in 1 BOTTLE (0436-0672-16) |
| NDC Code | 0436-0672-16 |
| Proprietary Name | Dakins Quarter |
| Package Description | 473 mL in 1 BOTTLE (0436-0672-16) |
| Product NDC | 0436-0672 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Hypochlorite |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060524 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Century Pharmaceuticals, Inc. |
| Substance Name | SODIUM HYPOCHLORITE |
| Strength Number | 1.25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |