Product NDC: | 13537-222 |
Proprietary Name: | Cyzone |
Non Proprietary Name: | Aluminum sesquichlorohydrate |
Active Ingredient(s): | 8.5 g/50mL & nbsp; Aluminum sesquichlorohydrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-222 |
Labeler Name: | Ventura Corporation Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111108 |
Package NDC: | 13537-222-50 |
Package Description: | 50 mL in 1 BOTTLE (13537-222-50) |
NDC Code | 13537-222-50 |
Proprietary Name | Cyzone |
Package Description | 50 mL in 1 BOTTLE (13537-222-50) |
Product NDC | 13537-222 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum sesquichlorohydrate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20111108 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ventura Corporation Limited |
Substance Name | ALUMINUM SESQUICHLOROHYDRATE |
Strength Number | 8.5 |
Strength Unit | g/50mL |
Pharmaceutical Classes |