| 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 |