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Esika
Esika - 13537-062-01 - (Aluminum Sesquichlorohydrate)
Drug Information of Esika
| Product NDC: | 13537-062 |
| Proprietary Name: | Esika |
| Non Proprietary Name: | Aluminum Sesquichlorohydrate |
| Active Ingredient(s): | .17 g/mL & nbsp; Aluminum Sesquichlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Esika
| Product NDC: | 13537-062 |
| Labeler Name: | Ventura Corporation Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111213 |
Package Information of Esika
| Package NDC: | 13537-062-01 |
| Package Description: | 50 mL in 1 BOTTLE (13537-062-01) |
NDC Information of Esika
| NDC Code | 13537-062-01 |
| Proprietary Name | Esika |
| Package Description | 50 mL in 1 BOTTLE (13537-062-01) |
| Product NDC | 13537-062 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Sesquichlorohydrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111213 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation Ltd. |
| Substance Name | ALUMINUM SESQUICHLOROHYDRATE |
| Strength Number | .17 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
