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nausea relief - 59779-407-26 - (Dextrose (glucose), Levulose (fructose), Phosphoric Acid)

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Drug Information of nausea relief

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)

Labeler Information of nausea relief

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 Information of nausea relief

Package NDC: 59779-407-26
Package Description: 1 BOTTLE in 1 CARTON (59779-407-26) > 118 mL in 1 BOTTLE

NDC Information of nausea relief

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

Complete Information of nausea relief


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