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Antibacterial
Antibacterial - 63691-002-02 - (Triclosan)
Drug Information of Antibacterial
| Product NDC: | 63691-002 |
| Proprietary Name: | Antibacterial |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .1 mL/100mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antibacterial
| Product NDC: | 63691-002 |
| Labeler Name: | Sun Products Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19980213 |
Package Information of Antibacterial
| Package NDC: | 63691-002-02 |
| Package Description: | 384 mL in 1 BOTTLE (63691-002-02) |
NDC Information of Antibacterial
| NDC Code | 63691-002-02 |
| Proprietary Name | Antibacterial |
| Package Description | 384 mL in 1 BOTTLE (63691-002-02) |
| Product NDC | 63691-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 19980213 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sun Products Corporation |
| Substance Name | TRICLOSAN |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
