Product NDC: | 13537-122 |
Proprietary Name: | CYZONE |
Non Proprietary Name: | Aluminum Sesquichlorohydrate |
Active Ingredient(s): | .2 g/mL & nbsp; Aluminum Sesquichlorohydrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-122 |
Labeler Name: | Ventura Corporation LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111114 |
Package NDC: | 13537-122-01 |
Package Description: | 50 mL in 1 BOTTLE, WITH APPLICATOR (13537-122-01) |
NDC Code | 13537-122-01 |
Proprietary Name | CYZONE |
Package Description | 50 mL in 1 BOTTLE, WITH APPLICATOR (13537-122-01) |
Product NDC | 13537-122 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum Sesquichlorohydrate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20111114 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ventura Corporation LTD |
Substance Name | ALUMINUM SESQUICHLOROHYDRATE |
Strength Number | .2 |
Strength Unit | g/mL |
Pharmaceutical Classes |