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anti nausea - 41250-291-26 - (Dextrose (glucose), Levulose (fructose), Phosphoric Acid)

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Drug Information of anti nausea

Product NDC: 41250-291
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: 41250-291
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19960821

Package Information of anti nausea

Package NDC: 41250-291-26
Package Description: 1 BOTTLE in 1 CARTON (41250-291-26) > 118 mL in 1 BOTTLE

NDC Information of anti nausea

NDC Code 41250-291-26
Proprietary Name anti nausea
Package Description 1 BOTTLE in 1 CARTON (41250-291-26) > 118 mL in 1 BOTTLE
Product NDC 41250-291
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 19960821
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Meijer Distribution Inc
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 anti nausea


General Information