Home › NDC Lookup › Ingredients › Acetaminophen, Dextromethorphan Hbr, Gua... › 11673-0691-12
Target Maximum Strength Cold Flu and Sore Throat Overnight Cold and Flu Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Triprolidine Kit — NDC 11673-0691-12 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Target Maximum Strength Cold Flu and Sore Throat Overnight Cold and Flu Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Triprolidine Kit — NDC 11673-691-12 (Billing 11673-0691-12)

by TARGET CORPORATION · 1 KIT in 1 CARTON * 180 mL in 1 BOTTLE * 180 mL in 1 BOTTLE

This is a package of Target Maximum Strength Cold Flu and Sore Throat Overnight Cold and Flu Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Triprolidine Kit from TARGET CORPORATION, marketed since Mar 2020 and currently FDA-listed. It is this product's only package size.

NDC 11673-0691-12
🏷️ FDA NDC (as labeled) 11673-691-12 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 11673-691-12 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
11673 labeler · 691 product · 12 package
Package marketed since
Mar 30, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0829576105779
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11673-691-12
Product NDC 11673-691
11-digit billing NDC 11673069112
RxCUI 1116572, 2173667, 2637729
UPC 0829576105779
Application # M012
SPL Set ID 6e94fdab-27ea-4c0f-a91c-735ce697304b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-03-30
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1116572
Why two NDCs? The FDA registers this code as 11673-691-12 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 11673-0691-12. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Anilides class.

Drug family (ATC) Anilides
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📖 About the active ingredient MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Acetaminophen is used to relieve mild to moderate pain and to reduce fever. Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Read the full MedlinePlus article ↗
🧪 What is this product?

This is an over-the-counter monograph kit containing multiple ingredients commonly used to relieve cold and flu symptoms. Acetaminophen is typically used to reduce fever and ease pain or aches. Dextromethorphan is a cough suppressant. Guaifenesin functions as an expectorant to help thin mucus. Phenylephrine and triprolidine work together as a decongestant and antihistamine to help relieve nasal congestion and other allergy-related symptoms associated with cold and flu.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
11673-0691-12 You're viewing this Main listing 1 KIT in 1 CARTON * 180 mL in 1 BOTTLE * 180 mL in 1 BOTTLE 2020-03-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Target Maximum Strength Cold Flu and Sore Throat Overnight Cold and Fluthis 11673-0691-12 TARGET 1 kit — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2020
On the market since
Mar 2020
📍
2026
Currently FDA-listed
6 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color blue
FlavorFruit
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

From the label’s inactive-ingredient sectionanhydrous citric acid, edetate disodium, FD&C Blue No.1, FD&C Red No. 40, flavors, potassium citrate, propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum 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 and xanthan gum

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerTARGET CORPORATION
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedMar 2020
Product typeHuman Otc Drug
Portfolio409 products on file

More NDCs from TARGET CORPORATION labeler code 11673

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🆘 Overdosage 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 111 words ▾

Uses MAXIMUM STRENGTH COLD, FLU & SORE THROAT temporarily relieves these common cold and flu symptoms: cough nasal congestion minor aches and pains sore throat headache stuffy nose sinus congestion and pressure temporarily reduces fever temporarily promotes nasal and for sinus drainage helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Uses (OVERNIGHT COLD & FLU 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

⏱️ Dosage and Administration 164 words ▾

Directions do not take more than directed (see Overdose warning) do not take more than 6 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 mL = milliliter adults and children 12 years of age and over: 20 mL in dosing cup provided every 4 hours children under 12 years of age: Do not use

Directions do not take more than directed (see overdose warnings 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 over: 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

⚠️ Warnings ~1 min read ▾

Warnings Liver warnings: This product contains acetaminophen. Severe liver damage may occur if you take: more than6 doses 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 warnings: 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.

Warnings Liver warnings: 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 If pregnant or breast feeding ask a health professional before use 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 Centre 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 Directions do not take more than directed (see overdose warnings 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 over: 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

🆘 Overdosage 51 words ▾

Overdose warnings. 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 don’t notice any signs or symptoms.

📦 Storage and Handling 16 words ▾

Other information each 20 mL contains: sodium 8 mg store at room temperature do not refrigerate

🧪 Active Ingredient 67 words ▾

Active ingredients (in each 20 mL) MAXIMUM STRENGTH ‡ COLD, FLU & SORE THROAT Purposes Acetaminophen 650 mg Dextromethorphan HBr 20 mg Pain reliever/fever reducer Cough suppressant Guaifenesin 400 mg Phenylephrine HCl 10 mg Expectorant Nasal decongestant Active ingredients (in each 20 mL) Purposes MAXIMUM STRENGTH OVERNIGHT COLD & FLU Acetaminophen 650 mg Pain reliever/fever reducer Dextromethorphan HBr 20 mg Triprolidine HCl 2.5 mg Cough suppressant Antihistamine

🧪 Inactive Ingredients 74 words ▾

Inactive ingredients (Maximum strength Cold, Flu and Sore Throat) anhydrous citric acid, edetate disodium, FD&C Blue No.1, FD&C Red No. 40, flavors, potassium citrate, propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Inactive ingredients (Overnight Cold & Flu) 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 and xanthan gum

🎯 Purpose 67 words ▾

Active ingredients (in each 20 mL) MAXIMUM STRENGTH ‡ COLD, FLU & SORE THROAT Purposes Acetaminophen 650 mg Dextromethorphan HBr 20 mg Pain reliever/fever reducer Cough suppressant Guaifenesin 400 mg Phenylephrine HCl 10 mg Expectorant Nasal decongestant Active ingredients (in each 20 mL) Purposes MAXIMUM STRENGTH OVERNIGHT COLD & FLU Acetaminophen 650 mg Pain reliever/fever reducer Dextromethorphan HBr 20 mg Triprolidine HCl 2.5 mg Cough suppressant Antihistamine

📄 Do Not Use 79 words ▾

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.

🤰 If Pregnant or Breast-Feeding 166 words ▾

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

If pregnant or breast feeding ask a health professional before use 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 Centre 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 Directions do not take more than directed (see overdose warnings 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 over: 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

📄 Keep Out of Reach of Children 62 words ▾

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 Centre 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

📄 Other Information 18 words ▾

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

📄 Questions or Comments 4 words ▾

Questions or comments? (1-866-467-2748)

📄 Package Label / Principal Display Panel ~1 min read ▾

PRINCIPAL DISPLAY PANEL - Kit Carton VALUE PACK NDC 11673-691-12 Compare to active ingredients Maximum Strength ‡ Mucinex® Fast Max® Cold, Flu and Sore Throat Maximum Strength ‡ Cold, Flu and Sore Throat Acetaminophen • Pain Reliever/Fever Reducer Dextromethorphan HBr • Cough Suppressant Guaifenesin • Expectorant Phenylephrine HCl • Nasal Decongestant Controls Cough, Thins & Loosens Mucus Nasal & Chest Congestion Sinus pressure & Congestion Body Pain, Headache, Fever & Sore Throat *Per 4-hour dose For Ages 12+ 6 FL.

OZ. (180 mL) *This product is not manufactured or distributed by Reckitt Benckiser, the distributor of Maximum Strength Mucinex® Fast-Max® Cold, Flu & Sore Throat. Compare to Mucinex® Nightshift Cold, Flu & Sore Throat Active Ingredients** Overnight Cold & Flu Acetaminophen • Pain Reliever/Fever Reducer Dextromethorphan HBr • Cough Suppressant Triprolidine HCl • Antihistamine Night Time Relief for a Better Morning Maximum Strength per 4-hour dose Cough Fever Sore Throat Runny Nose Sneezing For Ages 12+ 6 FL OZ (180 mL) **This product is not manufactured or distributed by RB Health, the distributor of Mucinex® Nightshift Cold & Flu.

TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING. See bottle for full labeling Distributed by: 094 14 8715 R00 C-001227-01-055 Dist. By Target Corp.

Mpls., MN 55403 TM & © 2020 Target Brands, Inc. Questions? Cal 1-866-467-2748 DO NOT TAKE MAXIMUM STRENGTH COLD, FLU & SORE THROAT & OVERNIGHT COLD & FLU LIQUIDS AT THE SAME TIME.

Target Max Strength Value Pack Cold and Flu Relief

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by TARGET CORPORATION. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TARGET CORPORATION is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 11673-0689-05 · Target 11673-0697-01 · TARGET →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.