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EQUALINE
EQUALINE - 41163-163-32 - (TRICLOSAN)
Drug Information of EQUALINE
| Product NDC: | 41163-163 |
| Proprietary Name: | EQUALINE |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .46 mg/100mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EQUALINE
| Product NDC: | 41163-163 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120626 |
Package Information of EQUALINE
| Package NDC: | 41163-163-32 |
| Package Description: | 946 mL in 1 BOTTLE, PLASTIC (41163-163-32) |
NDC Information of EQUALINE
| NDC Code | 41163-163-32 |
| Proprietary Name | EQUALINE |
| Package Description | 946 mL in 1 BOTTLE, PLASTIC (41163-163-32) |
| Product NDC | 41163-163 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | TRICLOSAN |
| Strength Number | .46 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
