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 |