| Product NDC: | 10096-0081 |
| Proprietary Name: | On Duty Original |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 207 mg/mL & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10096-0081 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121116 |
| Package NDC: | 10096-0081-2 |
| Package Description: | 75 mL in 1 BOTTLE, DISPENSING (10096-0081-2) |
| NDC Code | 10096-0081-2 |
| Proprietary Name | On Duty Original |
| Package Description | 75 mL in 1 BOTTLE, DISPENSING (10096-0081-2) |
| Product NDC | 10096-0081 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20121116 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 207 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |