| Product NDC: | 59779-306 | 
| Proprietary Name: | purelax | 
| Non Proprietary Name: | Polyethylene Glycol 3350 | 
| Active Ingredient(s): | 17 g/17g & nbsp; Polyethylene Glycol 3350 | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | POWDER, FOR SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-306 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA090685 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20091007 | 
| Package NDC: | 59779-306-04 | 
| Package Description: | 850 g in 1 BOTTLE (59779-306-04) | 
| NDC Code | 59779-306-04 | 
| Proprietary Name | purelax | 
| Package Description | 850 g in 1 BOTTLE (59779-306-04) | 
| Product NDC | 59779-306 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Polyethylene Glycol 3350 | 
| Dosage Form Name | POWDER, FOR SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20091007 | 
| Marketing Category Name | ANDA | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | POLYETHYLENE GLYCOL 3350 | 
| Strength Number | 17 | 
| Strength Unit | g/17g | 
| Pharmaceutical Classes |