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Anti Nausea
Anti Nausea - 37808-001-26 - (Dextrose (glucose), Levulose (fructose), Phosphoric Acid)
Drug Information of Anti Nausea
| Product NDC: | 37808-001 |
| 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: | 37808-001 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19951122 |
Package Information of Anti Nausea
| Package NDC: | 37808-001-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-001-26) > 118 mL in 1 BOTTLE |
NDC Information of Anti Nausea
| NDC Code | 37808-001-26 |
| Proprietary Name | Anti Nausea |
| Package Description | 1 BOTTLE in 1 CARTON (37808-001-26) > 118 mL in 1 BOTTLE |
| Product NDC | 37808-001 |
| 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 | 19951122 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | H E B |
| Substance Name | DEXTROSE; FRUCTOSE; PHOSPHORIC ACID |
| Strength Number | 1.87; 1.87; 21.5 |
| Strength Unit | g/5mL; g/5mL; mg/5mL |
| Pharmaceutical Classes |
