NDC 68737-238

ConRX DayTime

Phenylephrine Hydrochloride, Acetaminophen, Dextromethorphan Hydrobromide, And Guaifenesin

ConRX DayTime is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Eagle Distributors,inc. The primary component is Phenylephrine Hydrochloride; Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin.

Product ID68737-238_13b8d214-6167-49c7-bca3-acb3ea7515a5
NDC68737-238
Product TypeHuman Otc Drug
Proprietary NameConRX DayTime
Generic NamePhenylephrine Hydrochloride, Acetaminophen, Dextromethorphan Hydrobromide, And Guaifenesin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-01-31
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameEagle Distributors,Inc
Substance NamePHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active Ingredient Strength5 mg/1; mg/1; mg/1; mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 68737-238-22

50 POUCH in 1 BOX (68737-238-22) > 2 TABLET in 1 POUCH
Marketing Start Date2014-01-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68737-238-22 [68737023822]

ConRX DayTime TABLET
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-31
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
PHENYLEPHRINE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:edb1096e-30fa-46da-a498-d90fd5e05287
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1110988

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