| Product NDC: | 10565-066 |
| Proprietary Name: | Roll On Anti Perspirant |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 10 mg/100mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10565-066 |
| Labeler Name: | Hydrox Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111026 |
| Package NDC: | 10565-066-02 |
| Package Description: | 45 mL in 1 BOTTLE, WITH APPLICATOR (10565-066-02) |
| NDC Code | 10565-066-02 |
| Proprietary Name | Roll On Anti Perspirant |
| Package Description | 45 mL in 1 BOTTLE, WITH APPLICATOR (10565-066-02) |
| Product NDC | 10565-066 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111026 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hydrox Laboratories |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 10 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |