
USFDA APPLICATION NUMBER - 18983 / DOSAGE - FOR SOLUTION;ORAL - 360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/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**Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| POLYETHYLENE GLYCOL 3350(UNII: G2M7P15E5P) (POLYETHYLENE GLYCOL 3350 - UNII:G2M7P15E5P) | POLYETHYLENE GLYCOL 3350 | 240g in 4 |
| POTASSIUM CHLORIDE(UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM CHLORIDE | 2.98g in 4 |
| SODIUM BICARBONATE(UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) | SODIUM BICARBONATE | 6.72g in 4 |
| SODIUM CHLORIDE(UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) | SODIUM CHLORIDE | 5.84g in 4 |
| SODIUM SULFATE(UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37) | SODIUM SULFATE | 22.72g in 4 |