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ABLS
ABLS - 54473-109-08 - (Triclosan)
Drug Information of ABLS
| Product NDC: | 54473-109 |
| Proprietary Name: | ABLS |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .7458 g/237mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ABLS
| Product NDC: | 54473-109 |
| Labeler Name: | Melaleuca, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20060401 |
Package Information of ABLS
| Package NDC: | 54473-109-08 |
| Package Description: | 237 mL in 1 BOTTLE (54473-109-08) |
NDC Information of ABLS
| NDC Code | 54473-109-08 |
| Proprietary Name | ABLS |
| Package Description | 237 mL in 1 BOTTLE (54473-109-08) |
| Product NDC | 54473-109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20060401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Melaleuca, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | .7458 |
| Strength Unit | g/237mL |
| Pharmaceutical Classes |
