Mucus Relief DM Guaifenesin, Dextromethorphan HBr 600 mg; 30 mg Tablet, 20-count
by CVS Pharmacy · 20 BLISTER PACK in 1 CARTON (69842-933-20) / 1 TABLET in 1 BLISTER PACK
NDC 69842-0933-20
🏷️ FDA NDC (as labeled)
69842-933-20
billing pads the product segment with a zero
This package
Contains20-count
Pack sizes2 compare ↓
Also comes in:
40 tablets 69842-0933-40
OTC
Generic
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Aug 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
69842-933-20
Product NDC
69842-933
11-digit billing NDC
69842093320
RxCUI
1298324
UNII
495W7451VQ, 9D2RTI9KYH
UPC
0050428428429
Application #
ANDA209692
SPL Set ID
59c338a0-8dc9-43a7-b8df-c26ae475def3
Established class (EPC)
Expectorant
Physiologic effect
Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
Discontinued
FDA listing status
Discontinued by firm (certified through Aug 2026)
Marketing start
2019-02-28
Marketing end
2026-08-28
Route
ORAL
Dosage form
TABLET
Substance
GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
Why two NDCs?
The FDA registers this code as 69842-933-20 — 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 → 69842-0933-20. 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
LabelerCVS Pharmacy
Application holderAMNEAL PHARMACEUTICALS OF NEW YORK LLC
FDA applicationANDA209692 (ANDA)
Labeler code69842
First marketedFeb 2019
Product typeHuman Otc Drug
Portfolio550 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
📗 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?
Patient education
Supplement & herbal interactions
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.
💬 Questions about Guaifenesin, Dextromethorphan HBr?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 system | Per each | Per 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.
Try another pack size:
40 tablets
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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Mucus Relief DM Extended Release Caplets 600 mg/1; 30 mg 00536-1161-34 | Rugby | 20 tablets | $0.359 | — | Availability likely | — |
| Rugby Mucus Relief DM ER 30 mg/1; 600 mg 00536-1446-34 | Rugby | 20 tablets | $0.359 | — | Availability likely | — |
| Good Neighbor Pharmacy Mucus Dm 30 mg/1; 600 mg 46122-0817-61 | Amerisource | 20 tablets | $0.359 | — | Availability likely | — |
| Mucus Relief DM 600 mg/1; 30 mg 70000-0491-01 | CARDINAL | 20 tablets | $0.359 | — | Discontinued | — |
| Leader Mucus Relief DM 30 mg/1; 600 mg 70000-0722-01 | Cardinal | 20 tablets | $0.359 | — | Availability likely | — |
| Mucus Relief DM 600 mg/1; 30 mg 70677-1050-01 | Strategic | 1 tablet | $0.359 | — | Availability likely | — |
| Mucinex DM 600 mg/1; 30 mg 63824-0056-01 | Reckitt | 20 tablets | $0.608 | — | Discontinued | — |
| Good Sense Mucus DM 30 mg/1; 600 mg 00113-2219-01 | L. | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 00363-0474-01 | WALGREEN | 10 tablets | — | — | FDA listed | — |
| Mucus Relief DM Extended Release Caplets 600 mg/1; 30 mg 00363-0733-20 | Walgreens | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 30 mg/1; 600 mg 00363-3219-01 | Walgreen | 20 tablets | — | — | FDA listed | — |
| up and up mucus relief dm 30 mg/1; 600 mg 11673-0716-01 | Target | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 11822-0733-02 | Rite | 20 tablets | — | — | FDA listed | — |
| mucus relief DM 30 mg/1; 600 mg 11822-2219-00 | Rite | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM Extended Release Caplets 600 mg/1; 30 mg 17856-1162-01 | ATLANTIC | 1 tablet | — | — | FDA listed | — |
| Mucus Relief Dm 600 mg/1; 30 mg 21130-0997-67 | Better | 10 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 30142-0276-20 | KROGER | 10 tablets | — | — | FDA listed | — |
| Guaifenesin And Dextromethorphan Hbr 600 mg/1; 30 mg 30142-0948-20 | Kroger | 20 tablets | — | — | FDA listed | — |
| Topcare Mucus DM 30 mg/1; 600 mg 36800-0219-01 | Topco | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 37808-0733-40 | H | 40 tablets | — | — | FDA listed | — |
| equaline mucus dm 30 mg/1; 600 mg 41163-0599-01 | United | 20 tablets | — | — | FDA listed | — |
| mucus relief dm 30 mg/1; 600 mg 41250-0436-01 | Meijer | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 41415-0998-20 | PUBLIX | 20 tablets | — | — | FDA listed | — |
| Mucus Dm 30 mg/1; 600 mg 42507-0222-20 | HyVee | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBR 600 mg/1; 30 mg 43598-0114-01 | Dr. | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBR 600 mg/1; 30 mg 43598-0231-01 | Dr. | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 49035-0960-12 | Wal-Mart | 40 tablets | — | — | FDA listed | — |
| Mucinex Dm 600 mg/1; 30 mg 50090-1077-00 | A-S | 20 tablets | — | — | FDA listed | — |
| Mucinex DM 600 mg/1; 30 mg 50090-1078-00 | A-S | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBR 600 mg/1; 30 mg 51316-0009-01 | CVS | 20 tablets | — | — | FDA listed | — |
| Cough And Congestion Extended Release 600 mg/1; 30 mg 51316-0065-67 | CVS | 10 tablets | — | — | FDA listed | — |
| Mucus Relief Dm 30 mg/1; 600 mg 51316-0858-78 | CVS | 100 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 51660-0301-21 | OHM | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 55910-0733-06 | Dolgencorp, | 6 tablets | — | — | FDA listed | — |
| DG health mucus dm 30 mg/1; 600 mg 55910-0746-01 | Dolgencorp | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 58602-0714-05 | Aurohealth | 14 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 58602-0824-08 | Aurohealth | 10 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 58602-0871-83 | Aurohealth | 10 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 59726-0733-06 | P | 6 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 60000-0058-67 | Ahold | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 63304-0106-21 | SUN | 20 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 63941-0733-20 | Best | 20 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 65162-0038-03 | Amneal | 30 tablets | — | — | FDA listed | — |
| Mucinex DM, TRAVEL BASIX 600 mg/1; 30 mg 66715-6424-01 | Lil' | 2 tablets | — | — | FDA listed | — |
| Mucinex DM, CVP HEALTH 600 mg/1; 30 mg 66715-6524-01 | Lil' | 2 tablets | — | — | FDA listed | — |
| Mucinex DM 600 mg/1; 30 mg 66715-9724-01 | Lil' | 2 tablets | — | — | FDA listed | — |
| Mucus Relief DM Expectorant and Cough Suppressant 600 mg/1; 30 mg 67091-0314-20 | Winco | 10 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 67091-0344-20 | WinCo | 20 tablets | — | — | FDA listed | — |
| Mucinex DM 30 mg/1; 600 mg 67751-0171-01 | Navajo | 2 tablets | — | — | FDA listed | — |
| Mucus DM Extended Release 600 mg/1; 30 mg 69842-0057-11 | CVS | 10 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mgthis 69842-0933-20 | CVS | 20 tablets | — | — | Discontinued | — |
| mucus dm extended release 30 mg/1; 600 mg 69842-0963-01 | CVS | 20 tablets | — | — | FDA listed | — |
| Mucus Relief Dm 600 mg/1; 30 mg 72036-0012-20 | Harris | 10 tablets | — | — | FDA listed | — |
| basic care mucus dm 30 mg/1; 600 mg 72288-0219-49 | Amazon.com | 40 tablets | — | — | FDA listed | — |
| Amazon Basic Care Mucus Dm 600 mg/1; 30 mg 72288-0220-08 | Amazon.com | 10 tablets | — | — | FDA listed | — |
| Mucus Relief DM 600 mg/1; 30 mg 72476-0733-20 | Care | 20 tablets | — | — | FDA listed | — |
| equate mucus relief dm 30 mg/1; 600 mg 79903-0065-01 | Wal-Mart | 20 tablets | — | — | FDA listed | — |
| Mucinex DM 600 mg/1; 30 mg 85237-1650-01 | Select | 2 tablets | — | — | FDA listed | — |
| Guaifenesin and Dextromethorphan HBr 600 mg/1; 30 mg 85766-0150-14 | Sportpharm | 14 tablets | — | — | FDA listed | — |
| Good Sense Mucus DM 30 mg/1; 600 mg 85766-0172-20 | Sportpharm | 20 tablets | — | — | FDA listed | — |
| Mucinex DM 600 mg/1; 30 mg 85766-0176-20 | Sportpharm | 20 tablets | — | — | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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
🏛️
2019
On the market since
Feb 2019
📍
2026
Currently FDA-listed
7 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Mucus Relief DM (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 49%
Female · 51%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 69842-0933-20 You're viewing this | 20 BLISTER PACK in 1 CARTON (69842-933-20) / 1 TABLET in 1 BLISTER PACK | 2019-02-28 | Discontinued by firm |
| 69842-0933-40 | 40 BLISTER PACK in 1 CARTON (69842-933-40) / 1 TABLET in 1 BLISTER PACK | 2019-02-28 | Discontinued by firm |
Pack size FAQ
What quantity is in NDC 69842-0933-20?
NDC 69842-0933-20 is a 20-count package — 20 blister pack in 1 carton / 1 tablet in 1 blister pack.
What is the difference between NDC 69842-0933-20 and NDC 69842-0933-40?
Both are Mucus Relief DM Guaifenesin, Dextromethorphan HBr 600 mg; 30 mg Tablet — the drug itself is identical. NDC 69842-0933-20 is the 20-count package, while NDC 69842-0933-40 is the 40 tablets package.
What NDC number is used to bill for this package of Mucus Relief DM Guaifenesin, Dextromethorphan HBr 600 mg; 30 mg Tablet?
Bill NDC 69842-0933-20 — the 11-digit billing format is 69842093320. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
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
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 69842-933-20, 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: 69842-0933-20, written without dashes as 69842093320. 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 69842-0933-20, the first segment (69842) is the labeler code FDA assigned to CVS Pharmacy; the middle segment (0933) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (20) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 40 tablets (69842-0933-40). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
CVS Pharmacy 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 ▾
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 ▾
Directions do not crush, chew, or break tablet take with a full glass of water this product can be administered without regards for timing of meals adults and children 12 years of age and older: 1 or 2 tablet every 12 hours; not more than 4 tablets in 24 hours children under 12 years of age: do not use
⚠️ Warnings ▾
Warnings Do not use for children under12 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 (1-800-222-1222).
🧪 Active Ingredient ▾
Active ingredients (in each extended-release tablet) Dextromethorphan HBr 30 mg Guaifenesin 600 mg
🧪 Inactive Ingredients ▾
Inactive ingredients carbomer, colloidal silicon dioxide, D&Cyellow #10 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, talc
🎯 Purpose ▾
Purpose Cough Suppressant Expectorant
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.