Product NDC: | 53329-010 |
Proprietary Name: | Antiperspirant |
Non Proprietary Name: | aluminum chlorohydrate |
Active Ingredient(s): | 13 mL/100mL & nbsp; aluminum chlorohydrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53329-010 |
Labeler Name: | Medline Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 53329-010-13 |
Package Description: | 59 mL in 1 BOTTLE, SPRAY (53329-010-13) |
NDC Code | 53329-010-13 |
Proprietary Name | Antiperspirant |
Package Description | 59 mL in 1 BOTTLE, SPRAY (53329-010-13) |
Product NDC | 53329-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | aluminum chlorohydrate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medline Industries, Inc. |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 13 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |