Product NDC: | 10565-067 |
Proprietary Name: | Anti-Perspirant Deodorant |
Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
Active Ingredient(s): | 13 mg/100mL & nbsp; ALUMINUM CHLOROHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10565-067 |
Labeler Name: | Hydrox Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111111 |
Package NDC: | 10565-067-04 |
Package Description: | 118 mL in 1 BOTTLE, SPRAY (10565-067-04) |
NDC Code | 10565-067-04 |
Proprietary Name | Anti-Perspirant Deodorant |
Package Description | 118 mL in 1 BOTTLE, SPRAY (10565-067-04) |
Product NDC | 10565-067 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20111111 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Hydrox Laboratories |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 13 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |