NDC 11673-698 Target Overnight Cold And Flu
Acetaminophen, Dextromethorphan Hbr, Triprolidine Hcl Solution Oral

Product Information

Product Code11673-698
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Target Overnight Cold And Flu
Non-Proprietary Name 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.
Acetaminophen, Dextromethorphan Hbr, Triprolidine Hcl
Product Type 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.
Human Otc Drug
Dosage FormSolution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Target Corporation
Labeler Code11673
FDA Application Number 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.
Marketing Category 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.
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 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.
Exclude Flag 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".
NDC Code Structure

Usage Information

Product Characteristics

Color(s)BLUE (C48333)
Flavor(s)FRUIT (C73389)

Product Packages

NDC 11673-698-06

Package Description: 180 mL in 1 BOTTLE

Product Details

Target Overnight Cold And Flu is a human over the counter drug product labeled by Target Corporation. The generic name of Target Overnight Cold And Flu is acetaminophen, dextromethorphan hbr, triprolidine hcl. The product's dosage form is solution and is administered via oral form.

What are Target Overnight Cold And Flu Active Ingredients?

The following is the list of active ingredients in this product. An 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.

NDC to RxNorm Crosswalk

What is RxNorm? 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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

Inactive Ingredient(s)

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.

  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • WATER (UNII: 059QF0KO0R)
  • SORBITOL (UNII: 506T60A25R)

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Target Overnight Cold And Flu Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents


Drug Facts

Otc - Purpose

Active ingredients (in each 20 mL)Purposes

Acetaminophen 650 mg

Pain reliever/fever reducer

Dextromethorphan HBr 20 mg

Cough suppressant

Triprolidine HCl 2.5 mg



  • ▪temporarily relieves these common cold and flu symptoms:
    • ▪cough
    • ▪minor aches and pains
    • ▪sore throat
    • ▪headache
    • ▪runny nose
    • ▪sneezing
    • ▪itching of the nose or throat
    • ▪itchy, watery eyes due to hay fever
    • ▪temporarily reduces fever
    • ▪controls cough to help you get to sleep

Liver Warning

This product contains acetaminophen. Severe liver damage may occur if you take:

  • ▪more than 4000 mg in 24 hours, which is the maximum daily amount
  • ▪with other drugs containing acetaminophen
  • ▪3 or more alcoholic drinks daily while using this product

Allergy Alert

Acetaminophen may cause severe skin reactions. Symptoms may include:

  • ▪skin reddening
  • ▪blisters
  • ▪rash
  • If a skin reaction occurs, stop use and seek medical help right away.

Sore Throat Warning

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do Not Use

  • ▪with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • ▪if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask A Doctor Before Use If You Have

  • ▪liver disease
  • ▪glaucoma
  • ▪trouble urinating due to an enlarged prostate gland
  • ▪a breathing problem such as emphysema or chronic bronchitis
  • ▪persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • ▪cough that occurs with too much phlegm (mucus)

Ask A Doctor Or Pharmacist Before Use If You Are

  • ▪taking the blood thinning drug warfarin
  • ▪taking sedatives or tranquilizers

When Using This Product

  • do not use more than directed
  • ▪excitability may occur, especially in children
  • ▪marked drowsiness may occur
  • ▪alcohol, sedatives, and tranquilizers may increase drowsiness
  • ▪avoid alcoholic drinks
  • ▪use caution when driving a motor vehicle or operating machinery

Stop Use And Ask A Doctor If

  • ▪pain or cough gets worse or lasts more than 7 days
  • ▪fever gets worse or lasts more than 3 days
  • ▪redness or swelling is present
  • ▪new symptoms occur
  • ▪cough comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Overdose Warning

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


  • do not take more than directed (see Overdose warning)
  • ▪do not take more than 4 doses in any 24-hour period
  • ▪measure only with dosing cup provided
  • ▪do not use dosing cup with other products
  • ▪dose as follows or as directed by a doctor
  • adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours
  • children under 12 years of age: do not use

Other Information

  • each 20 mL contains: sodium 10 mg
  • ▪low sodium
  • ▪store at room temperature
  • ▪do not refrigerate

Inactive Ingredients

anhydrous citric acid, ascorbic acid, edetate disodium, FD&C Blue No. 1, FD&C Red No. 40, flavors, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Questions Or Comments?


Principal Display Panel - 180 Ml Bottle Label

Compare to Mucinex® Nightshift Cold & Flu Active Ingredients*

NDC 11673-698-06

Overnight Cold & Flu

Acetaminophen – Pain Reliever/Fever Reducer
Dextromethorphan HBr – Cough Suppressant
Triprolidine HCl – Antihistamine

Night Time
Relief for a Better Morning

  • •Cough
  • •Fever
  • •Sore throat
  • •Runny nose
  • •Sneezing
  • 6 FL OZ (180 mL)For Ages 12+

    Tamper evident: do not use if printed seal under cap is broken or missing

    Maximum Strength per 4-hour dose

    Distributed by:

    Target Corp.

    Mpls., MN 55403

    *This product is not manufactured or distributed by RB Health, the distributor of Mucinex® Nightshift Cold & Flu.

* Please review the disclaimer below.