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anti nausea
anti nausea - 11822-0207-4 - (Dextrose (glucose), Levulose (fructose), Phosphoric Acid)
Drug Information of anti nausea
| Product NDC: | 11822-0207 |
| Proprietary Name: | anti nausea |
| 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) |
Labeler Information of anti nausea
| Product NDC: | 11822-0207 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19960612 |
Package Information of anti nausea
| Package NDC: | 11822-0207-4 |
| Package Description: | 1 BOTTLE in 1 CARTON (11822-0207-4) > 118 mL in 1 BOTTLE |
NDC Information of anti nausea
| NDC Code | 11822-0207-4 |
| Proprietary Name | anti nausea |
| Package Description | 1 BOTTLE in 1 CARTON (11822-0207-4) > 118 mL in 1 BOTTLE |
| Product NDC | 11822-0207 |
| 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 | 19960612 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rite Aid Corporation |
| Substance Name | DEXTROSE; FRUCTOSE; PHOSPHORIC ACID |
| Strength Number | 1.87; 1.87; 21.5 |
| Strength Unit | g/5mL; g/5mL; mg/5mL |
| Pharmaceutical Classes |
