| Product NDC: | 0904-5666 |
| Proprietary Name: | phosphate |
| Non Proprietary Name: | dibasic sodium phosphate, monobasic sodium phosphate |
| Active Ingredient(s): | 2.9; 7.2 g/15mL; g/15mL & nbsp; dibasic sodium phosphate, monobasic sodium phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0904-5666 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100602 |
| Package NDC: | 0904-5666-75 |
| Package Description: | 1 BOTTLE in 1 CARTON (0904-5666-75) > 45 mL in 1 BOTTLE |
| NDC Code | 0904-5666-75 |
| Proprietary Name | phosphate |
| Package Description | 1 BOTTLE in 1 CARTON (0904-5666-75) > 45 mL in 1 BOTTLE |
| Product NDC | 0904-5666 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dibasic sodium phosphate, monobasic sodium phosphate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100602 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC |
| Strength Number | 2.9; 7.2 |
| Strength Unit | g/15mL; g/15mL |
| Pharmaceutical Classes |