NDC 63824-251

Mucinex Sinus-Max Day Night

Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, And Diphenhydramine Hydrochloride

Mucinex Sinus-Max Day Night is a Kit in the Human Otc Drug category. It is labeled and distributed by Rb Health (us) Llc. The primary component is .

Product ID63824-251_60cff976-38d2-4905-97df-059914815749
NDC63824-251
Product TypeHuman Otc Drug
Proprietary NameMucinex Sinus-Max Day Night
Generic NameAcetaminophen, Guaifenesin, Phenylephrine Hydrochloride, And Diphenhydramine Hydrochloride
Dosage FormKit
Marketing Start Date2018-11-20
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameRB Health (US) LLC
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63824-251-01

1 KIT in 1 PACKAGE, COMBINATION (63824-251-01) * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2018-11-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63824-251-01 [63824025101]

Mucinex Sinus-Max Day Night KIT
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-11-20

Drug Details

OpenFDA Data

SPL SET ID:e964d32f-7ed2-44a9-901e-50df011ef697
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 1939343
  • 1233575
  • 1243679

    • NDC Crossover Matching brand name "Mucinex Sinus-Max Day Night" or generic name "Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, And Diphenhydramine Hydrochloride"

    NDCBrand NameGeneric Name
    63824-202Mucinex Sinus-Max Day NightAcetaminophen, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride
    63824-251Mucinex Sinus-Max Day NightAcetaminophen, Guaifenesin, Phenylephrine Hydrochloride, and Diphenhydramine Hydrochloride
    63824-204Mucinex Sinus-Max Day NightMucinex Sinus-Max Day Night
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