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Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide 1200 mg; 60 mg Tablet, Extended Release, 7-count — NDC 63824-0072-07 package photo

Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide 1200 mg; 60 mg Tablet, Extended Release, 7-count

by Reckitt Benckiser LLC · 1 BLISTER PACK in 1 CARTON (63824-072-07) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
NDC 63824-0072-07
🏷️ FDA NDC (as labeled) 63824-072-07 billing pads the product segment with a zero
This package
Contains7-count Cost per ea$0.9123 NADAC Per package$6.39 / 7 tablets Pack sizes7 compare ↓
Also comes in: 1 tablet 63824-0072-02 12 tablets 63824-0072-48 14 tablets 63824-0072-35 14 tablets 63824-0072-36 14 tablets 63824-0072-46 14 tablets 63824-0072-56
OTC Brand On market Non-controlled
🗂️ Data synced Sep 17, 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) 63824-072-07
Product NDC 63824-072
11-digit billing NDC 63824007207
NCPDP billing unit EA — each (per item)
RxCUI 1099074
UNII 495W7451VQ, 9D2RTI9KYH
UPC 0363824072142
Application # NDA021620
SPL Set ID 588eddc1-fa30-41cc-8ed9-c01319ea21c6
Established class (EPC) Expectorant
Physiologic effect Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions
DEA schedule Non-controlled
Marketing category NDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2012-06-26
Route ORAL
Dosage form TABLET, EXTENDED RELEASE
Substance GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
GPI-14 43997002527475
GPI class Mucinex DM Maximum Strength
GCN Seq No 042105
GCN 93677
HICL code 000223
Ingredient (HICL) Guaifenesin/Dextromethorphan
HIC1 code B
Therapeutic class — broad (HIC1) Respiratory System
HIC2 code B3
Therapeutic class — intermediate (HIC2) Drugs Affecting Primarily The Trachea And Bronchi
HIC3 code B3T
Therapeutic class — specific (HIC3) Non-Opioid Antitussive And Expectorant Combination
AHFS code 48:08.00.00
AHFS class Antitussives
FDB label name MUCINEX DM ER 1,200-60 MG TAB
FDB brand name Mucinex Dm
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 63824-072-07 — 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 → 63824-0072-07. 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 Uncompetitive N-methyl-D-aspartate Receptor Antagonist class.

Pharmacologic class Uncompetitive N-methyl-D-aspartate Receptor Antagonist, Sigma-1 Agonist
Drug family (ATC) Other antidepressants, Opium alkaloids and derivatives
How it works Uncompetitive NMDA Receptor Antagonists, Sigma-1 Receptor Agonists
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

LabelerReckitt Benckiser LLC
Application holderRECKITT BENCKISER LLC
FDA applicationNDA021620 (NDA)
Labeler code63824
First marketedJun 2012
Product typeHuman Otc Drug
Portfolio174 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 MUCINEX DM ER 1,200-60 MG TAB Ingredient Guaifenesin/Dextromethorphan
📖 What it is MedlinePlus · NLM

Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • The two ingredients tackle your symptoms from different angles. Guaifenesin is an expectorant — it helps thin and loosen the mucus in your chest so you can cough it up more easily....
  • What exactly does this combination do — why are two ingredients needed?
  • It depends on which antidepressant you're taking. If it's a type called an MAOI — which includes certain older antidepressants and some medications for Parkinson's disease — you sh...
  • Can I take this if I'm on an antidepressant?
📖 Read our full Dextromethorphan / Guaifenesin guide →

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.

💊 What it looks like

Color white
ShapeOval
ImprintMucinex;1200
Size22 mm
ScoringNot scored
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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII HHT01ZNK31
    Carbomer Homopolymer Type B is a synthetic polymer made from acrylic acid. It absorbs water and forms a gel, so it's used in medicines as a thickener, suspending agent, and to help create a smooth texture in creams, gels, and lotions.
  • UNII 35SW5USQ3G
    A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
  • UNII 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statescarbomer homopolymer type B; D&C yellow no. 10 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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 eaPer package
Retail pharmacies payNADAC · weekly $0.912 $6.39 / 7 tablets
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.
NADAC price history (per ea) — tap or hover for the price & month
Dec 2023 $0.912 $0.912
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
Maximum Strength Guaifenesin DM 60 mg/1; 1200 mg 00536-1213-88 Rugby 14 tablets $0.546 — Availability likely save 40%
Rugby Mucus Relief Dm Er 1200 mg/1; 60 mg 00536-1447-88 Rugby 14 tablets $0.546 — Availability likely save 40%
good neighbor pharmacy mucus dm 1200 mg/1; 60 mg 46122-0637-03 Amerisource 28 tablets $0.546 — Availability likely save 40%
Mucus Relief DM Extended Release Caplets 60 mg/1; 1200 mg 70000-0464-01 Cardinal 28 tablets $0.546 — Availability likely save 40%
Mucus Relief DM 60 mg/1; 1200 mg 70677-1049-01 Strategic 1 tablet $0.546 — Availability likely save 40%
Mucus Relief DM 60 mg/1; 1200 mg 83324-0137-14 QUALITY 1 tablet $0.546 — Availability likely save 40%
Mucinex DM Maximum Strength 1200 mg/1; 60 mgthis 63824-0072-07 Reckitt 7 tablets $0.912 — FDA listed —
Robitussin Maximum Strength 12 Hour Cough and Mucus Relief 60 mg/1; 1200 mg 00031-8765-04 Haleon 4 tablets — — FDA listed —
good sense mucus dm 1200 mg/1; 60 mg 00113-0812-03 L 1 tablet — — FDA listed —
Mucus Relief DM Extended Release Caplets Maximum Strength 60 mg/1; 1200 mg 00363-0437-14 Walgreens 14 tablets — — FDA listed —
Maximum Strength Mucus Relief DM 1200 mg/1; 60 mg 00363-0510-65 WALGREEN 7 tablets — — FDA listed —
mucus relief dm 1200 mg/1; 60 mg 00363-6812-30 Walgreen 28 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 11673-0267-05 Target 14 tablets — — FDA listed —
mucus relief DM MAX 1200 mg/1; 60 mg 11822-1812-00 Rite 14 tablets — — FDA listed —
Mucus Relief DM Maximum Strength 60 mg/1; 1200 mg 11822-7340-04 Rite 42 tablets — — FDA listed —
Guaifenesin and Dextromethorphan Hydrobromide HBR 1200 mg/1; 60 mg 11822-9996-01 RITE-AID 14 tablets — — FDA listed —
Mucus Relief DM MAXIMUM STRENGTH 1200 mg/1; 60 mg 21130-0989-03 Better 7 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 30142-0275-05 KROGER 7 tablets — — FDA listed —
Guaifenesin And Dextromethorphan Hbr 1200 mg/1; 60 mg 30142-0963-14 Kroger 14 tablets — — FDA listed —
Topcare Mucus DM 1200 mg/1; 60 mg 36800-0592-30 Topco 28 tablets — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 37808-0730-42 H 42 tablets — — FDA listed —
mucus relief dm 60 mg/1; 1200 mg 37808-0812-66 H 14 tablets — — Discontinued —
Mucus Relief DM 60 mg/1; 1200 mg 37808-0834-14 H 14 tablets — — FDA listed —
Equaline Mucus DM 1200 mg/1; 60 mg 41163-0781-66 United 14 tablets — — FDA listed —
mucus dm 1200 mg/1; 60 mg 41250-0812-30 Meijer 28 tablets — — Discontinued —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 41415-0999-14 PUBLIX 14 tablets — — FDA listed —
mucus dm 60 mg/1; 1200 mg 42507-0812-66 HyVee 14 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBR 1200 mg/1; 60 mg 43598-0115-28 Dr. 7 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBR 1200 mg/1; 60 mg 43598-0232-37 Dr. 14 tablets — — FDA listed —
Mucus DM 1200 mg/1; 60 mg 46122-0420-03 Amerisource 7 tablets — — FDA listed —
Mucus Relief DM Extended Release Caplets 60 mg/1; 1200 mg 49035-0824-28 EQUATE 28 tablets — — FDA listed —
Maximum Strength Mucus Relief DM 1200 mg/1; 60 mg 49035-0956-61 Wal-Mart 28 tablets — — FDA listed —
Mucus Relief DM Extended Release Caplets 60 mg/1; 1200 mg 50090-6020-00 A-S 14 tablets — — FDA listed —
Mucinex DM Maximum Strength 1200 mg/1; 60 mg 50090-6549-00 A-S 14 tablets — — FDA listed —
Good Sense Mucus Dm 1200 mg/1; 60 mg 50090-7258-00 A-S 14 tablets — — FDA listed —
Rugby Mucus Relief Dm Er 1200 mg/1; 60 mg 50090-7891-00 A-S 14 tablets — — FDA listed —
Maximum Strength Cough And Congestion Extended Release 1200 mg/1; 60 mg 51316-0060-65 CVS 7 tablets — — FDA listed —
Guaifenesin and Dextromethorphan Hydrobromide 1200 mg/1; 60 mg 51316-0600-70 CVS 14 tablets — — FDA listed —
Mucus Relief Dm 1200 mg/1; 60 mg 51316-0671-55 CVS 42 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 51660-0110-54 OHM 14 tablets — — FDA listed —
Exchange Select Mucus DM 1200 mg/1; 60 mg 55301-0812-66 Army 14 tablets — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 55319-0734-07 Family 1 tablet — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 55319-0741-14 Family 1 tablet — — FDA listed —
DG health mucus dm 1200 mg/1; 60 mg 55910-0575-03 Dolgencorp, 1 tablet — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 58602-0715-05 Aurohealth 14 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 58602-0825-06 Aurohealth 7 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 58602-0849-11 Aurohealth 7 tablets — — FDA listed —
Mucus Relief DM 1200 mg/1; 60 mg 60000-0057-65 Ahold 14 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 63304-0110-54 SUN 14 tablets — — FDA listed —
Mucus Relief DM Extended Release Caplets 60 mg/1; 1200 mg 63868-0870-14 QUALITY 14 tablets — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 63941-0734-14 Best 14 tablets — — FDA listed —
kirkland signature mucus dm 60 mg/1; 1200 mg 63981-0812-01 Costco 84 tablets — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 65162-0039-03 Amneal 30 tablets — — FDA listed —
Mucus Relief DM Expectorant and Cough Suppressant Maximum Strength 1200 mg/1; 60 mg 67091-0315-14 Winco 7 tablets — — FDA listed —
Mucus Relief DM Maximum Strength 60 mg/1; 1200 mg 67091-0345-14 WinCo 14 tablets — — FDA listed —
Mucus Relief DM Maximum Strength 60 mg/1; 1200 mg 68016-0674-14 Chain 14 tablets — — FDA listed —
members mark mucus relief dm 1200 mg/1; 60 mg 68196-0812-45 Sam's 56 tablets — — FDA listed —
Members Mark Mucus Relief DM 1200 mg/1; 60 mg 68196-0999-56 SAM'S 14 tablets — — FDA listed —
Berkley and Jensen Mucus Relief DM 1200 mg/1; 60 mg 68391-0812-45 BJWC 56 tablets — — FDA listed —
Maximum Strength Mucus DM Extended Release 1200 mg/1; 60 mg 69842-0059-10 CVS 7 tablets — — FDA listed —
mucus dm extended release 1200 mg/1; 60 mg 69842-0812-30 CVS 28 tablets — — Discontinued —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 71179-0011-21 VESPYR 7 tablets — — FDA listed —
Mucus Relief DM 1200 mg/1; 60 mg 72036-0980-65 Harris 7 tablets — — FDA listed —
basic care mucus dm 1200 mg/1; 60 mg 72288-0812-55 Amazon.com 42 tablets — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 72476-0734-14 Care 14 tablets — — FDA listed —
Mucus Relief - Dm Maximum Strength 60 mg/1; 1200 mg 73581-0405-98 YYBA 98 tablets — — FDA listed —
Mucus Relief - Dm Maximum Strength 60 mg/1; 1200 mg 73581-0406-01 YYBA 100 tablets — — FDA listed —
Guaifenesin And Dextromethorphan Hbr 1200 mg/1; 60 mg 76162-0032-56 TOPCO 7 tablets — — FDA listed —
Mucus Relief DM 60 mg/1; 1200 mg 81522-0734-14 FSA 1 tablet — — FDA listed —
Guaifenesin and Dextromethorphan HBr 1200 mg/1; 60 mg 85766-0046-28 Sportpharm 7 tablets — — FDA listed —
About this product: this is the brand-name version. Some generic versions are approved by the FDA, but we could not confirm current pharmacy availability from our pricing/market data.
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

🏛️
2012
On the market since
Jun 2012
📍
2026
Currently FDA-listed
14 years listed
🔒
·
Generic approved (availability unconfirmed)
see note
🔒Generic approved by FDA, but pharmacy availability is not confirmed

The FDA lists approved generic versions of this medicine, but that does not always mean a pharmacy can get one today. Patent rules, launch agreements, supply and pricing can affect when generics actually arrive.

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 Per unit Per pack Marketing startStatus
63824-0072-02 1 POUCH in 1 CARTON (63824-072-02) / 1 TABLET, EXTENDED RELEASE in 1 POUCH — — 2021-08-01 Active
63824-0072-07 You're viewing this 1 BLISTER PACK in 1 CARTON (63824-072-07) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK $0.9123 / ea $6.39 2012-06-26 Active
63824-0072-35 1 BLISTER PACK in 1 CARTON (63824-072-35) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK $0.9123 / ea $12.77 2012-06-26 Active
63824-0072-36 2 BLISTER PACK in 1 CARTON (63824-072-36) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK $0.9123 / ea $25.55 2012-06-26 Active
63824-0072-46 3 BLISTER PACK in 1 CARTON (63824-072-46) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK $0.9123 / ea $38.32 2012-06-26 Active
63824-0072-48 4 BLISTER PACK in 1 CARTON (63824-072-48) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK — — 2012-06-26 Active
63824-0072-56 4 BLISTER PACK in 1 CARTON (63824-072-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK $0.9123 / ea $51.09 2021-07-01 Active

This pack has the lowest per-ea cost of the 5 priced pack sizes ($0.9123 NADAC).

Pack size FAQ

What quantity is in NDC 63824-0072-07?
NDC 63824-0072-07 is a 7-count package — 1 blister pack in 1 carton / 7 tablet, extended release in 1 blister pack.
What is the difference between NDC 63824-0072-07 and NDC 63824-0072-02?
Both are Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide 1200 mg; 60 mg Tablet, Extended Release — the drug itself is identical. NDC 63824-0072-07 is the 7-count package, while NDC 63824-0072-02 is the 1 tablet package.
What NDC number is used to bill for this package of Mucinex DM Maximum Strength Guaifenesin and Dextromethorphan Hydrobromide 1200 mg; 60 mg Tablet, Extended Release?
Bill NDC 63824-0072-07 — the 11-digit billing format is 63824007207. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

📄 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 56 words ▾

Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep

⏱️ Dosage and Administration 58 words ▾

Directions do not crush, chew, or break extended-release tablet take with a full glass of water this product can be administered without regard for timing of meals adults and children 12 years and older: 1 extended-release tablet every 12 hours; not more than 2 extended-release tablets in 24 hours children under 12 years of age: do not use

⚠️ Warnings 164 words ▾

Warnings Do not use for children under 12 years of age 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 persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus) When using this product do not use more than directed Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache.

These could be signs of a serious illness. 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.

📦 Storage and Handling 6 words ▾

Other information store at 20-25°C (68-77°F)

🧪 Active Ingredient 30 words ▾

Active ingredients (in each extended-release tablet) Dextromethorphan HBr 60 mg Guaifenesin 1200 mg Active ingredients (in each extended-release tablet) Purposes Dextromethorphan HBr 60 mg Cough suppressant Guaifenesin 1200 mg Expectorant

🧪 Inactive Ingredients 24 words ▾

Inactive ingredients carbomer homopolymer type B; D&C yellow no. 10 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

🎯 Purpose 17 words ▾

Active ingredients (in each extended-release tablet) Purposes Dextromethorphan HBr 60 mg Cough suppressant Guaifenesin 1200 mg Expectorant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 63824-0057-18 · Reckitt 63824-0115-66 · Reckitt →
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.