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esika
esika - 13537-506-01 - (Aluminum Chlorohydrate)
Drug Information of esika
| Product NDC: | 13537-506 |
| Proprietary Name: | esika |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | .045 g/mL & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of esika
| Product NDC: | 13537-506 |
| Labeler Name: | Ventura Corporation LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130527 |
Package Information of esika
| Package NDC: | 13537-506-01 |
| Package Description: | 125 mL in 1 BOTTLE, SPRAY (13537-506-01) |
NDC Information of esika
| NDC Code | 13537-506-01 |
| Proprietary Name | esika |
| Package Description | 125 mL in 1 BOTTLE, SPRAY (13537-506-01) |
| Product NDC | 13537-506 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130527 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation LTD. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | .045 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
