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Original - 22431-529-01 - (Triclosan)
Drug Information of Original
| Product NDC: | 22431-529 |
| Proprietary Name: | Original |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .46 mL/100mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Original
| Product NDC: | 22431-529 |
| Labeler Name: | Blue Cross Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110722 |
Package Information of Original
| Package NDC: | 22431-529-01 |
| Package Description: | 222 mL in 1 BOTTLE (22431-529-01) |
NDC Information of Original
| NDC Code | 22431-529-01 |
| Proprietary Name | Original |
| Package Description | 222 mL in 1 BOTTLE (22431-529-01) |
| Product NDC | 22431-529 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110722 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Blue Cross Laboratories, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .46 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
