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Equaline
Equaline - 41163-220-08 - (TRICLOSAN)
Drug Information of Equaline
| Product NDC: | 41163-220 |
| Proprietary Name: | Equaline |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .15 mL/100mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Equaline
| Product NDC: | 41163-220 |
| Labeler Name: | Supervalu Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101007 |
Package Information of Equaline
| Package NDC: | 41163-220-08 |
| Package Description: | 222 mL in 1 BOTTLE (41163-220-08) |
NDC Information of Equaline
| NDC Code | 41163-220-08 |
| Proprietary Name | Equaline |
| Package Description | 222 mL in 1 BOTTLE (41163-220-08) |
| Product NDC | 41163-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20101007 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Supervalu Inc |
| Substance Name | TRICLOSAN |
| Strength Number | .15 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
