
USFDA APPLICATION NUMBER - 22204 / DOSAGE - GEL;TRANSDERMAL - 10% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| OXYBUTYNIN CHLORIDE(UNII: L9F3D9RENQ) (OXYBUTYNIN - UNII:K9P6MC7092) | OXYBUTYNIN CHLORIDE | 100mg in 1 |
Inactive Ingredients
| Ingredient Name | Actavis Pharma, Inc. |
|---|---|
| ALCOHOL(3K9958V90M) | |
| GLYCERIN(PDC6A3C0OX) | |
| HYDROXYPROPYL CELLULOSE (TYPE H)(RFW2ET671P) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| WATER(059QF0KO0R) |