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Night Time Cherry - 70253-113-06 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)

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Drug Information of Night Time Cherry

Product NDC: 70253-113
Proprietary Name: Night Time Cherry
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Active Ingredient(s): 500; 15; 6.25    mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Night Time Cherry

Product NDC: 70253-113
Labeler Name: Nash-Finch Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20051108

Package Information of Night Time Cherry

Package NDC: 70253-113-06
Package Description: 177 mL in 1 BOTTLE, PLASTIC (70253-113-06)

NDC Information of Night Time Cherry

NDC Code 70253-113-06
Proprietary Name Night Time Cherry
Package Description 177 mL in 1 BOTTLE, PLASTIC (70253-113-06)
Product NDC 70253-113
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20051108
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Nash-Finch Company
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 500; 15; 6.25
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Night Time Cherry


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