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Sunmark Day time - 49348-753-37 - (acetaminophen, dextromethorphan Hbr, Phenylephrine HCl)

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Drug Information of Sunmark Day time

Product NDC: 49348-753
Proprietary Name: Sunmark Day time
Non Proprietary Name: acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Active Ingredient(s): 325; 10; 5    mg/15mL; mg/15mL; mg/15mL & nbsp;   acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Day time

Product NDC: 49348-753
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060609

Package Information of Sunmark Day time

Package NDC: 49348-753-37
Package Description: 237 mL in 1 BOTTLE (49348-753-37)

NDC Information of Sunmark Day time

NDC Code 49348-753-37
Proprietary Name Sunmark Day time
Package Description 237 mL in 1 BOTTLE (49348-753-37)
Product NDC 49348-753
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060609
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Sunmark Day time


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