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: | 10096-0081-1 |
Package Description: | 50 mL in 1 BOTTLE, DISPENSING (10096-0081-1) |
NDC Code | 10096-0081-1 |
Proprietary Name | On Duty Original |
Package Description | 50 mL in 1 BOTTLE, DISPENSING (10096-0081-1) |
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 |