41250-473 NDC - DAYTIME COUGH ()

Drug Information

  • Product NDC: 41250-473
  • Proprietary Name: daytime cough
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Meijer Distribution Inc
Product Type:
FDA Application Number: M012
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:8/15/2007
End Marketing Date:2/28/2022

Package Information

No. Package Code Package Description Billing Unit
141250-473-38296 mL in 1 BOTTLE (41250-473-38)
241250-473-40355 mL in 1 BOTTLE (41250-473-40)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41250-473The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAMEdaytime coughThis is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME SUFFIXnon drowsyThis 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.
START MARKETING DATE8/15/2007An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
END MARKETING DATE2/28/2022 
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM012This 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 NAMEMeijer Distribution IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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