| Product NDC: | 50007-3000 |
| Proprietary Name: | Lactovit Men Roll-On Antiperspirant Deodorant |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 15 mL/100mL & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50007-3000 |
| Labeler Name: | Antonio Puig, S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091216 |
| Package NDC: | 50007-3000-1 |
| Package Description: | 50 mL in 1 BOTTLE (50007-3000-1) |
| NDC Code | 50007-3000-1 |
| Proprietary Name | Lactovit Men Roll-On Antiperspirant Deodorant |
| Package Description | 50 mL in 1 BOTTLE (50007-3000-1) |
| Product NDC | 50007-3000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20091216 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Antonio Puig, S.A. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 15 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |