| Product NDC: | 10096-9182 | 
| Proprietary Name: | Black Suede | 
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE | 
| Active Ingredient(s): | 7.25 mL/50mL & nbsp; ALUMINUM CHLOROHYDRATE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | GEL | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 10096-9182 | 
| Labeler Name: | Avon Products, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part350 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20110128 | 
| Package NDC: | 10096-9182-1 | 
| Package Description: | 50 mL in 1 BOTTLE, DISPENSING (10096-9182-1) | 
| NDC Code | 10096-9182-1 | 
| Proprietary Name | Black Suede | 
| Package Description | 50 mL in 1 BOTTLE, DISPENSING (10096-9182-1) | 
| Product NDC | 10096-9182 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE | 
| Dosage Form Name | GEL | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110128 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Avon Products, Inc. | 
| Substance Name | ALUMINUM CHLOROHYDRATE | 
| Strength Number | 7.25 | 
| Strength Unit | mL/50mL | 
| Pharmaceutical Classes |