NDC 49580-0155

Flu Relief Therapy Day Time

Theraflu Daytime

Flu Relief Therapy Day Time is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by P & L Development, Llc. The primary component is Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.

Product ID49580-0155_97fad820-aabf-428b-ae77-d6c61c08a80c
NDC49580-0155
Product TypeHuman Otc Drug
Proprietary NameFlu Relief Therapy Day Time
Generic NameTheraflu Daytime
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-12-11
Marketing End Date2021-12-30
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameP & L Development, LLC
Substance NameACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength325 mg/15mL; mg/15mL; mg/15mL
NDC Exclude FlagN

Packaging

NDC 49580-0155-8

237 mL in 1 BOTTLE, PLASTIC (49580-0155-8)
Marketing Start Date2013-12-11
Marketing End Date2021-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49580-0155-8 [49580015508]

Flu Relief Therapy Day Time LIQUID
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-12-11
Marketing End Date2021-12-30

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/15mL

OpenFDA Data

SPL SET ID:b79d0ebb-04f4-4a81-ba30-e2b29dfc3078
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1113705
  • UPC Code
  • 0715256808064
  • NDC Crossover Matching brand name "Flu Relief Therapy Day Time" or generic name "Theraflu Daytime"

    NDCBrand NameGeneric Name
    11822-2104Flu Relief Therapy Day TimeAcetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride
    49580-0155Flu Relief Therapy Day TimeTheraflu Daytime
    68016-155Flu Relief Therapy Day TimeAcetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

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