| Product NDC: | 59779-407 | 
| Proprietary Name: | nausea relief | 
| Non Proprietary Name: | Dextrose (glucose), Levulose (fructose), Phosphoric Acid | 
| Active Ingredient(s): | 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL & nbsp; Dextrose (glucose), Levulose (fructose), Phosphoric Acid | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-407 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 19960530 | 
| Package NDC: | 59779-407-26 | 
| Package Description: | 1 BOTTLE in 1 CARTON (59779-407-26) > 118 mL in 1 BOTTLE | 
| NDC Code | 59779-407-26 | 
| Proprietary Name | nausea relief | 
| Package Description | 1 BOTTLE in 1 CARTON (59779-407-26) > 118 mL in 1 BOTTLE | 
| Product NDC | 59779-407 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Dextrose (glucose), Levulose (fructose), Phosphoric Acid | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 19960530 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | DEXTROSE; FRUCTOSE; PHOSPHORIC ACID | 
| Strength Number | 1.87; 1.87; 21.5 | 
| Strength Unit | g/5mL; g/5mL; mg/5mL | 
| Pharmaceutical Classes |