| Product NDC: | 13537-441 |
| Proprietary Name: | esika MEN Control Fresh Deodorant and Antiperspirant |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | .045 g/mL & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13537-441 |
| Labeler Name: | Ventura Corporation LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121204 |
| Package NDC: | 13537-441-01 |
| Package Description: | 125 mL in 1 BOTTLE, PLASTIC (13537-441-01) |
| NDC Code | 13537-441-01 |
| Proprietary Name | esika MEN Control Fresh Deodorant and Antiperspirant |
| Package Description | 125 mL in 1 BOTTLE, PLASTIC (13537-441-01) |
| Product NDC | 13537-441 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121204 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation LTD. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | .045 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |