1. Home
  2. Labeler Index
  3. Target Corporation
  4. NDC Product Code: 11673-848 Daytime Nighttime Ultra Concentrated Cold And Flu

NDC 11673-848 Daytime Nighttime Ultra Concentrated Cold And Flu

Daytime - Acetaminophen,Dextromethrophan Hbr,Phenylephrine Hcl And Nighttime - - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 11673-848?
  5. Daytime Nighttime Ultra Concentrated Cold And Flu Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
11673-848
Proprietary Name:
Daytime Nighttime Ultra Concentrated Cold And Flu
Non-Proprietary Name: [1]
Daytime - Acetaminophen, Dextromethrophan Hbr, Phenylephrine Hcl And Nighttime - Acetaminophen, Dextromethrophan Hbr, Doxylamine Succinate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Product Label ID:
0c0cf76f-2dd3-45ef-e063-6394a90a9fef
FDA Application Number: [6]
M012
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
05-01-2024
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
GREEN (C48329)
Shape:
OVAL (C48345)
Size(s):
15 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 11673-848?

The NDC code 11673-848 is assigned by the FDA to the product Daytime Nighttime Ultra Concentrated Cold And Flu which is a human over the counter drug product labeled by Target Corporation. The generic name of Daytime Nighttime Ultra Concentrated Cold And Flu is daytime - acetaminophen, dextromethrophan hbr, phenylephrine hcl and nighttime - acetaminophen, dextromethrophan hbr, doxylamine succinate. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 11673-848-83 1 kit in 1 carton * 48 capsule, liquid filled in 1 bottle * 48 capsule, liquid filled in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Daytime Nighttime Ultra Concentrated Cold And Flu?

• take only as directed• do not exceed 8 LiquiCaps per 24 hrsadults & children 12 yrs & over2 LiquiCaps with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use • take only as directed• do not exceed 8 LiquiCaps per 24 hrsadults & children 12 yrs & over2 LiquiCaps with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Which are Daytime Nighttime Ultra Concentrated Cold And Flu UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Daytime Nighttime Ultra Concentrated Cold And Flu Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Daytime Nighttime Ultra Concentrated Cold And Flu?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1426334 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1426334 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Oral Capsule

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This 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.

[8] What is the Marketing Category? - Product 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".