| Product NDC: | 13537-359 |
| Proprietary Name: | CYZONE |
| Non Proprietary Name: | Aluminum Sesquichlorohydrate |
| Active Ingredient(s): | .17 mL/mL & nbsp; Aluminum Sesquichlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13537-359 |
| Labeler Name: | Ventura Corporation (San Juan, P.R) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110527 |
| Package NDC: | 13537-359-01 |
| Package Description: | 50 mL in 1 BOTTLE (13537-359-01) |
| NDC Code | 13537-359-01 |
| Proprietary Name | CYZONE |
| Package Description | 50 mL in 1 BOTTLE (13537-359-01) |
| Product NDC | 13537-359 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Sesquichlorohydrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110527 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation (San Juan, P.R) |
| Substance Name | ALUMINUM SESQUICHLOROHYDRATE |
| Strength Number | .17 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |