63824-511 NDC - MAXIMUM STRENGTH MUCINEX FAST-MAX DAY TIME COLD AND FLU AND NIGHT TIME COLD AND FLU ()

Drug Information

  • Product NDC: 63824-511
  • Proprietary Name: Maximum Strength Mucinex Fast-Max Day Time Cold and Flu and Night Time Cold and Flu
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: RB Health (US) LLC
Product Type:
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:7/28/2018

Package Information

No. Package Code Package Description Billing Unit
163824-511-101 KIT in 1 CARTON (63824-511-10) * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACK
263824-511-202 KIT in 1 CARTON (63824-511-20) / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACKEA
363824-511-301 KIT in 1 CARTON (63824-511-30) * 1 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACKEA
463824-511-404 KIT in 1 CARTON (63824-511-40) / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC63824-511The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMaximum Strength Mucinex Fast-Max Day Time Cold and Flu and Night Time Cold and FluThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart341This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMERB Health (US) LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC63824-511The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMaximum Strength Mucinex Fast-Max Day Time Cold and Flu and Night Time Cold and FluThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/28/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart341This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMERB Health (US) LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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