Home › NDC Lookup › Ingredients › Acetaminophen Dextromethorphan Hbr Pheny... › 00067-8127-08
🧴image loading
(from DailyMed)

Theraflu ExpressMax Daytime Severe Cold and Cough Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl 650 mg/30mL; 20 mg/30mL; 10 mg/30mL Syrup, 245.5 mL

by Haleon US Holdings LLC · 245.5 mL in 1 BOTTLE (0067-8127-08)
NDC 00067-8127-08
🏷️ FDA NDC (as labeled) 0067-8127-08 billing pads the labeler segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 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

🆔 Identity & classification

FDA NDC (as labeled) 0067-8127-08
Product NDC 0067-8127
11-digit billing NDC 00067812708
NCPDP billing unit ML — per mL (volume)
RxCUI 1113705
UNII 362O9ITL9D, 9D2RTI9KYH, 04JA59TNSJ
Application # M012
SPL Set ID ff48b55a-0d32-47d6-941d-d99c7cf52f94
Established class (EPC) Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Mechanism of action Adrenergic alpha1-Agonists; Sigma-1 Receptor Agonists; Uncompetitive NMDA Receptor Antagonists
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-07-15
Route ORAL
Dosage form SYRUP
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
GPI-14 43996903400910
GPI class Theraflu ExpressMax
GCN Seq No 061337
GCN 97129
HICL code 008885
Ingredient (HICL) D-Methorphan/Pe/Acetaminophen
HIC1 code B
Therapeutic class — broad (HIC1) Respiratory System
HIC2 code B4
Therapeutic class — intermediate (HIC2) Drugs Affecting The Trachea And Bronchi (Contin.1)
HIC3 code B4M
Therapeutic class — specific (HIC3) Non-Opioid Antitussive-Decongestant-Analgesic Comb
AHFS code 12:12.04.00
AHFS class Alpha-Adrenergic Agonists (12:12)
FDB label name THERAFLU EXPRESSMAX COLD-COUGH
FDB brand name Theraflu Expressmax Cold-Cough
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 0067-8127-08 — a 4-4-2 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 labeler segment → 00067-8127-08. 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.

🏭 Manufacturer & labeler

LabelerHaleon US Holdings LLC
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code00067
First marketedJul 2015
Product typeHuman Otc Drug
Portfolio405 products on file
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.

🩺 Clinical

Label name THERAFLU EXPRESSMAX COLD-COUGH Ingredient D-Methorphan/Pe/Acetaminophen
🧪 What is this product?

Theraflu ExpressMax Daytime Severe Cold and Cough is an over-the-counter liquid syrup taken by mouth. It contains acetaminophen, commonly used as a pain reliever and fever reducer; dextromethorphan, typically used to relieve cough; and phenylephrine, commonly used as a nasal decongestant. This combination product is formulated for daytime use in people seeking relief from multiple cold and cough symptoms.

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.

🧪 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.

💲 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 mLPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Leader Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 70000-0191-01 Cardinal 237 ml $0.013 — FDA listed —
Good Sense Daytime non drowsy cold and flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 00113-0656-34 L. 237 ml $0.014 — Availability likely —
foster and thrive daytime cold and flu relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 70677-1031-01 Strategic 237 ml $0.014 — Availability likely —
Theraflu ExpressMax Daytime Severe Cold and Cough 650 mg/30mL; 20 mg/30mL; 10 mg/30mLthis 00067-8127-08 Haleon 245.5 ml — — FDA listed —
Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 00363-0666-34 Walgreen 237 ml — — FDA listed —
Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 00363-4661-12 Walgreens 355 ml — — Discontinued —
Cold and Flu Day 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 00363-9912-02 Walgreen 355 ml — — FDA listed —
Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 00363-9974-08 Walgreens 237 ml — — FDA listed —
Daytime Cold and Flu 5 mg/15mL; 325 mg/15mL; 10 mg/15mL 11673-0765-01 TARGET 354 ml — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 11822-1583-01 Rite 237 ml — — Discontinued —
Day Time Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 21130-0580-08 Safeway, 237 ml — — FDA listed —
Day Time Cold and Flu Relief non drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 21130-0866-08 Safeway, 237 ml — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 5 mg/15mL; 10 mg/15mL 21130-0947-06 BETTER 236 ml — — FDA listed —
Good Neighbor Pharmacy Day Time 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 24385-0005-30 Amerisource 177 ml — — Discontinued —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 30142-0666-12 The 355 ml — — Discontinued —
topcare day time cold and flu relief multi symptom relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 36800-0522-34 Topco 237 ml — — FDA listed —
DayTime 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 37808-0656-38 H 296 ml — — Discontinued —
Daytime Severe Cold and Cough 650 mg/30mL; 20 mg/30mL; 10 mg/30mL 37808-0718-83 H 245 ml — — FDA listed —
Cold and Flu Daytime 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 37835-0526-02 Bi-Mart 355 ml — — FDA listed —
Daytime Cold And Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 37835-0527-12 BI-MART 355 ml — — FDA listed —
equaline daytime cold and flu relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 41163-0656-40 United 355 ml — — FDA listed —
Daytime Cold and Flu 5 mg/15mL; 10 mg/15mL; 325 mg/15mL 41226-0772-01 Kroger 354 ml — — FDA listed —
Daytime cold and flu non drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 41250-0656-40 Meijer 355 ml — — FDA listed —
CareOne DayTime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 41520-0032-34 American 237 ml — — Discontinued —
Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 42507-0522-40 HyVee 355 ml — — FDA listed —
Daytime Cold and Flu Non drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 49035-0466-12 EQUATE 355 ml — — FDA listed —
equate daytime cold and flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 49035-0726-40 Wal-Mart 355 ml — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 49580-0466-01 P 296 ml — — FDA listed —
Severe Cold and Cough Relief Daytime 650 mg/30mL; 20 mg/30mL; 10 mg/30mL 49580-0501-08 P 245 ml — — FDA listed —
Tukol Honey Daytime Cold and Flu 21.667 mg/mL; .667 mg/mL; .333 mg/mL 50066-0302-04 Genomma 1 bottle — — FDA listed —
Cold and Flu Daytime Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 50844-0251-02 L.N.K. 355 ml — — Discontinued —
daytime cold and flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 51316-0350-34 CVS 1 bottle — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 51316-0466-08 CVS 237 ml — — FDA listed —
Daytime Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 51316-0617-12 CVS 354 ml — — FDA listed —
DAY-TIME Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 53942-0506-28 DeMoulas 354 ml — — FDA listed —
Day-Time COLD/FLU RELIEF 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 53943-0506-28 Discount 354 ml — — FDA listed —
Cold and Flu Daytime 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 55301-0712-02 ARMY 355 ml — — FDA listed —
Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 55319-0646-12 Family 355 ml — — FDA listed —
Daytime Cold and Flu 650 mg/30mL; 20 mg/30mL; 10 mg/30mL 55319-0960-08 Family 245 ml — — FDA listed —
Sanatos Multi Symptom Daytime 10 mg/15mL; 5 mg/15mL; 325 mg/15mL 55758-0055-25 Pharmadel 177 ml — — FDA listed —
Cold and Flu Relief Daytime 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 55910-0366-12 Dolgencorp, 355 ml — — FDA listed —
DG Health Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 55910-0656-34 Dolgencorp 237 ml — — FDA listed —
Severe Cold and Cough Relief Daytime 650 mg/30mL; 20 mg/30mL; 10 mg/30mL 55910-0801-08 Dolgencorp, 245 ml — — FDA listed —
day time non drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 56062-0656-40 Publix 355 ml — — FDA listed —
Daytime Non-Drowsy COLD/FLU 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 57243-0506-25 Salado 177 ml — — FDA listed —
Daytime Non Drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 59779-0656-34 CVS 237 ml — — FDA listed —
Daytime Cold and Flu Non Drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 63868-0020-08 QUALITY 237 ml — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 63941-0466-06 Best 177 ml — — FDA listed —
Circle K Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 66715-5531-04 Lil' 237 ml — — FDA listed —
Daytime Cold and Flu Relief, 24-7 Life BY 7-Eleven 10 mg/15mL; 325 mg/15mL; 5 mg/15mL 66715-6415-04 Lil' 355 ml — — FDA listed —
DayTime Relief, Cold and Flu, 24-7 Life by 7-Eleven 5 mg/15mL; 10 mg/15mL; 325 mg/15mL 66715-6615-04 Lil' 177 ml — — FDA listed —
Daytime Cold and Flu Lil Drug Store Products 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 66715-6931-04 Lil' 237 ml — — FDA listed —
Cold and Flu Relief Multi symptom 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 67091-0287-54 WinCo 355 ml — — FDA listed —
Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 67091-0471-12 WinCo 355 ml — — FDA listed —
Daytime Cold and Flu Non drowsy 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 69256-0466-12 Harris 355 ml — — FDA listed —
Vicks DayQuil Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 69423-0788-04 The 118 ml — — FDA listed —
Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 71141-0179-32 Lidl 355 ml — — FDA listed —
Basic Care Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 72288-0656-34 Amazon.com 237 ml — — FDA listed —
XL-3 Day Time 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 76281-0304-28 AptaPharma 354 ml — — FDA listed —
XL-3 Day Time 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 76281-0306-25 AptaPharma 177 ml — — FDA listed —
Day-Time Cold/Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 76281-0506-25 AptaPharma 177 ml — — FDA listed —
Daytime Cold and Flu 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 83324-0167-12 QUALITY 355 ml — — FDA listed —
Cold and Flu Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 83324-0168-08 QUALITY 237 ml — — FDA listed —
Vicks DayQuil Cold and Flu Multi-Symptom Relief 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 84126-0315-04 The 118 ml — — FDA listed —
Revasol Daytime Cold And Flu 10 mg/30mL; 20 mg/30mL; 650 mg/30mL 84379-0275-04 Rnv 118 ml — — FDA listed —
XL-3 Day Time 10 mg/15mL; 325 mg/15mL; 5 mg/15mL 84379-0441-06 Rnv 177 ml — — FDA listed —
Daytime Cold and Flu 5 mg/15mL; 10 mg/15mL; 325 mg/15mL 85828-0772-01 Grocery 354 ml — — 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

🏛️
2015
On the market since
Jul 2015
📍
2026
Currently FDA-listed
11 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
00067-8127-08 You're viewing this 245.5 mL in 1 BOTTLE (0067-8127-08) 2015-07-15 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 FDA registers it as 0067-8127-08, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 00067-8127-08, written without dashes as 00067812708. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 00067-8127-08, the first segment (00067) is the labeler code FDA assigned to Haleon US Holdings LLC; the middle segment (8127) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Haleon US Holdings LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Haleon US Holdings LLC 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.

📄 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 40 words ▾

Uses • temporarily relieves these symptoms due to a cold: • minor aches and pains • minor sore throat pain • headache • nasal and sinus congestion • cough due to minor throat and bronchial irritation • temporarily reduces fever

⏱️ Dosage and Administration 70 words ▾

Directions • do not use more than directed • measure the dose correctly using the enclosed dosing cup • take every 4 hours in dosing cup provided, while symptoms persist • do not take more than 5 doses (150 mL) in 24 hours unless directed by a doctor Age Dose adults and children 12 years of age and over 30 mL children under 12 years of age do not use

⚠️ Warnings ~2 min read ▾

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take • more than 4,000 mg of acetaminophen in 24 hours • with other drugs containing acetaminophen • 3 or more alcoholic drinks every day 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 • in a child under 12 years of age • if you are allergic to acetaminophen • 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 • heart disease • high blood pressure • thyroid disease • diabetes • trouble urinating due to an enlarged prostate gland • cough that occurs with too much phlegm (mucus) • cough that lasts or is chronic such as occurs with smoking, asthma or emphysema Ask a doctor or pharmacist before use if you are • taking the blood thinning drug warfarin When using this product • do not exceed recommended dosage Stop use and ask a doctor if • nervousness, dizziness, or sleeplessness occurs • fever gets worse or lasts more than 3 days • redness or swelling is present • new symptoms occur • pain, cough or nasal congestion gets worse or lasts more than 7 days • cough comes back or occurs with rash or headache that lasts.

These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

🧪 Active Ingredient 17 words ▾

Active ingredients (in each 30 mL) Acetaminophen 650 mg Dextromethorphan HBr 20 mg Phenylephrine HCl 10 mg

🧪 Inactive Ingredients 29 words ▾

Inactive ingredients acesulfame potassium, anhydrous citric acid, edetate disodium, FD&C blue no. 1, FD&C red no. 40, flavors, glycerin, maltitol solution, propylene glycol, purified water, sodium benzoate, sodium citrate

🎯 Purpose 8 words ▾

Purposes Pain reliever/fever reducer Cough suppressant Nasal decongestant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 00067-8125-16 · Haleon 00067-8129-08 · Haleon →
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.