Home › NDC Lookup › Ingredients › Dextromethorphan Hbr Guaifenesin › 41520-0931-34
careone tussin dm Dextromethorphan HBr, Guaifenesin 20 mg/20mL; 400 mg/20mL Solution — NDC 41520-0931-34 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

careone tussin dm Dextromethorphan HBr, Guaifenesin 20 mg/20mL; 400 mg/20mL Solution — NDC 41520-931-34 (Billing 41520-0931-34)

by American Sales Company · 1 BOTTLE in 1 CARTON / 237 mL in 1 BOTTLE

This is a package of careone tussin dm Dextromethorphan HBr, Guaifenesin 20 mg/20mL; 400 mg/20mL Solution from American Sales Company, no longer marketed (first marketed Sep 2018), no longer in the FDA NDC Directory.

NDC 41520-0931-34
🏷️ FDA NDC (as labeled) 41520-931-34 billing pads the product segment with a zero
This package
Contains237 mL in 1 bottle Pack sizes2 compare ↓
Product page 41520-0931-26 Also comes in: 118 mL 41520-931-26
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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 41520-931-34 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41520 labeler · 931 product · 34 package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4152093134 5
FDA record last changed
Oct 1, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41520-931-34
Product NDC 41520-931
11-digit billing NDC 41520093134
RxCUI 1020138
UNII 9D2RTI9KYH, 495W7451VQ
Application # M012
SPL Set ID 6c90fccf-0e6f-43df-9468-d8ece8ded009
Established class (EPC) Expectorant
Physiologic effect Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2018-09-20
Route ORAL
Dosage form SOLUTION
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Quick answers
  • RxCUI (RxNorm): 1020138
Why two NDCs? The FDA registers this code as 41520-931-34 — 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 → 41520-0931-34. 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.

Clinical

📖 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
  • It helps loosen mucus and makes coughs more productive. It also temporarily eases cough from minor throat and bronchial irritation, like with a cold or inhaled irritants.
  • Swallow them whole with a full glass of water. Don’t crush, chew or break them. You can take them with or without food, about every 12 hours as your label directs.
  • How do I take the extended-release tablets?
  • The extended-release tablets are not for children under 12. Some liquid products are made for children, so check that product’s label and ask me if you’re unsure.
📖 Read our full Dextromethorphan / Guaifenesin guide →
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 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.
Try another pack size: 118 mL
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
41520-0931-26 41520-931-26 Main listing 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE 2018-09-20 — Active
41520-0931-34 You're viewing this 1 BOTTLE in 1 CARTON / 237 mL in 1 BOTTLE 2018-09-20 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle in 1 carton / 237 ml in 1 bottle.
What NDC number is used to bill for this package of careone tussin dm Dextromethorphan HBr, Guaifenesin 20 mg/20mL; 400 mg/20mL Solution?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
good neighbor pharmacy tussin dm max 20 mg/20mL; 400 mg/20mL 46122-0541-34 Amerisource 1 bottle $0.018 — Availability likely —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 70000-0565-01 Cardinal 177 ml $0.020 — Discontinued —
Mucus Relief DM 20 mg/20mL; 400 mg/20mL 70000-0707-01 Cardinal 177 ml $0.021 — Availability likely —
QCH Maximum Strength Mucus Relief DM 628 20 mg/20mL; 400 mg/20mL 83324-0026-06 Chain 177 ml $0.021 — Availability likely —
Good Sense Tussin DM Max 20 mg/20mL; 400 mg/20mL 00113-0927-26 L. 1 bottle $0.023 — Availability likely —
Good Neighbor Childrens Cough Relief Cherry Flavor 5 mg/5mL; 100 mg/5mL 46122-0786-29 AMERISOURCE 1 bottle $0.023 — Availability likely —
Tussin DM 20 mg/20mL; 400 mg/20mL 70000-0628-01 Cardinal 1 bottle $0.023 — Availability likely —
Foster and Thrive Adult Tussin DM MAX 20 mg/20mL; 400 mg/20mL 70677-1036-01 Strategic 1 bottle $0.023 — Availability likely —
Childrens Delsym Cough Plus Chest Congestion DM 5 mg/5mL; 100 mg/5mL 63824-0214-64 Reckitt 1 bottle $0.059 — FDA listed —
Mucinex Childrens Cough 5 mg/5mL; 100 mg/5mL 63824-0946-03 Reckitt 1 bottle $0.059 — FDA listed —
Delsym Cough Plus Chest Congestion DM 20 mg/20mL; 400 mg/20mL 63824-0213-66 Reckitt 180 ml $0.062 — FDA listed —
Mucinex Fast-Max DM Max Honey and Berry Flavor 20 mg/20mL; 400 mg/20mL 63824-0535-66 Reckitt 180 ml $0.062 — FDA listed —
Robitussin Elderberry Maximum Strength Cough plus Chest Congestion DM 20 mg/20mL; 400 mg/20mL 00031-2097-01 Haleon 1 bottle — — FDA listed —
Childrens Robitussin Elderberry Cough and Chest Congestion DM 20 mg/20mL; 400 mg/20mL 00031-2098-01 Haleon 1 bottle — — FDA listed —
Childrens Robitussin Cough and Chest Congestion DM 5 mg/5mL; 100 mg/5mL 00031-8715-10 Haleon 1 bottle — — FDA listed —
Robitussin Maximum Strength Cough Plus Chest Congestion Dm 20 mg/20mL; 400 mg/20mL 00031-8739-12 Haleon 1 bottle — — FDA listed —
Robitussin Honey Maximum Strength Cough and Chest Congestion DM 20 mg/20mL; 400 mg/20mL 00031-8756-12 Haleon 1 bottle — — FDA listed —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 00363-0505-06 Walgreens 177 ml — — Discontinued —
Cough and Chest Congestion DM Maximum Strength 20 mg/20mL; 400 mg/20mL 00363-0506-06 Walgreens 177 ml — — FDA listed —
tussin dm max 20 mg/20mL; 400 mg/20mL 00363-1144-26 Walgreen 1 bottle — — FDA listed —
Mucus Relief Cough Childrens 5 mg/5mL; 100 mg/5mL 00363-5527-04 Walgreens 1 bottle — — FDA listed —
Mucus Relief DM Honey and Berry Flavor 20 mg/20mL; 400 mg/20mL 00363-6005-06 WALGREENS 180 ml — — FDA listed —
Walgreen Cough and Chest Congestion 20 mg/20mL; 400 mg/20mL 00363-7296-06 WALGREEN 180 ml — — FDA listed —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 00363-7390-06 WALGREENS 180 ml — — FDA listed —
Walgreens Daytime Childrens 5 mg/5mL; 100 mg/5mL 00363-7550-04 WALGREENS 118 ml — — FDA listed —
Adult Cough plus Chest Congestion DM with Honey 20 mg/20mL; 400 mg/20mL 00363-7754-04 WALGREEN 1 bottle — — FDA listed —
DM Max 20 mg/20mL; 400 mg/20mL 00363-8031-45 Walgreen 177 ml — — FDA listed —
7 Select Maximum Strength 20 mg/20mL; 400 mg/20mL 10202-0740-04 7-ELEVEN 1 bottle — — FDA listed —
up and up cough plus chest congestion 20 mg/20mL; 400 mg/20mL 11673-0627-26 Target 1 bottle — — Discontinued —
tussin cough chest congestion 20 mg/20mL; 400 mg/20mL 11822-1332-01 Rite 1 bottle — — FDA listed —
Mucus DM 20 mg/20mL; 400 mg/20mL 11822-5050-06 Rite 177 ml — — Discontinued —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 21130-0505-06 Safeway, 177 ml — — Discontinued —
tussin 20 mg/20mL; 400 mg/20mL 21130-0707-26 Safeway 1 bottle — — FDA listed —
Mucus Relief DM 20 mg/20mL; 400 mg/20mL 30142-0508-06 The 177 ml — — FDA listed —
tussin dm max 20 mg/20mL; 400 mg/20mL 30142-0843-26 Kroger 1 bottle — — FDA listed —
Mucus Relief DM Max Maximum Strength 20 mg/20mL; 400 mg/20mL 36800-0605-06 TOP 177 ml — — FDA listed —
topcare tussin dm max 20 mg/20mL; 400 mg/20mL 36800-0847-26 Topco 1 bottle — — FDA listed —
Maximum Strength DM MAX 20 mg/20mL; 400 mg/20mL 37808-0518-25 H 177 ml — — FDA listed —
Mucus Relief Cough Childrens 5 mg/5mL; 100 mg/5mL 37808-0594-04 H 1 bottle — — FDA listed —
tussin 20 mg/20mL; 400 mg/20mL 37808-0639-26 H 1 bottle — — FDA listed —
equaline tussin 20 mg/20mL; 400 mg/20mL 41163-0704-26 United 1 bottle — — FDA listed —
KROGER Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 41226-0739-06 KROGER 180 ml — — FDA listed —
adult dm max cough and chest congestion 20 mg/20mL; 400 mg/20mL 41250-0261-34 Meijer 1 bottle — — FDA listed —
Meijer Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 41250-0748-06 MEIJER, 180 ml — — FDA listed —
careone tussin dm 20 mg/20mL; 400 mg/20mLthis 41520-0931-34 American 1 bottle — — Discontinued —
Maximum Strength Mucus Relief 20 mg/20mL; 400 mg/20mL 42507-0630-58 Hyvee 177 ml — — FDA listed —
Good Neighbor Pharmacy Mucus Relief Dm Maximum Strength 20 mg/20mL; 400 mg/20mL 46122-0840-29 AMERISOURCE 180 ml — — FDA listed —
equate adult tussin dm max 20 mg/20mL; 400 mg/20mL 49035-0705-26 Wal-Mart 1 bottle — — FDA listed —
Childrens Cough 5 mg/5mL; 100 mg/5mL 49035-0773-03 Wal-Mart 1 bottle — — FDA listed —
Maximum Strength Mucus Relief DM 20 mg/20mL; 400 mg/20mL 49035-0839-06 Wal-Mart 180 ml — — FDA listed —
Tussin DM Max 20 mg/20mL; 400 mg/20mL 49035-0930-19 Wal-Mart 1 bottle — — FDA listed —
Tussin DM Daytime 20 mg/20mL; 400 mg/20mL 51316-0304-19 CVS 1 bottle — — FDA listed —
Cough and Chest Congestion DM Daytime 20 mg/20mL; 400 mg/20mL 51316-0305-19 CVS 1 bottle — — FDA listed —
DM Maximum 20 mg/20mL; 400 mg/20mL 51316-0310-45 CVS 177 ml — — FDA listed —
Cough and Chest Congestion DM 20 mg/20mL; 400 mg/20mL 51316-0389-45 CVS 177 ml — — FDA listed —
Cough and Congestion 20 mg/20mL; 400 mg/20mL 51316-0500-19 CVS 1 bottle — — FDA listed —
Childrens Mucus and Cough Relief 5 mg/5mL; 100 mg/5mL 51316-0552-03 CVS 1 bottle — — FDA listed —
CVS Maximum Strength 20 mg/20mL; 400 mg/20mL 51316-0740-04 CVS 1 bottle — — FDA listed —
CVS Adult Cough plus Chest Congestion DM Max with Honey 20 mg/20mL; 400 mg/20mL 51316-0775-08 CVS 1 bottle — — FDA listed —
daytime cough and chest congestion dm 20 mg/20mL; 400 mg/20mL 51316-0826-26 CVS 1 bottle — — FDA listed —
Pediacare Childrens Cough and Congestion Grape 5 mg/5mL; 100 mg/5mL 52412-0992-01 RANDOB 1 bottle — — FDA listed —
Maximum strength Tussnex FM DM Max 20 mg/20mL; 400 mg/20mL 53041-0628-58 Guardian 177 ml — — FDA listed —
DM Max CONGESTION and COUGH 20 mg/20mL; 400 mg/20mL 53942-0518-25 DeMoulas 177 ml — — FDA listed —
Childrens Cough Mucus Relief 5 mg/5mL; 100 mg/5mL 53943-0512-24 Discount 118 ml — — FDA listed —
Maxium Strength Dm Max 20 mg/20mL; 400 mg/20mL 53943-0518-25 Discount 117 ml — — FDA listed —
Mucus Relief DM Max 20 mg/20mL; 400 mg/20mL 55319-0731-45 Family 177 ml — — FDA listed —
Maximum Strength Adult Cough plus Chest Congestion DM 20 mg/20mL; 400 mg/20mL 55319-0740-04 FAMILY 1 bottle — — FDA listed —
Childrens Mucus and Cough Relief 5 mg/5mL; 100 mg/5mL 55319-0924-03 Family 1 bottle — — FDA listed —
SanaTos Children Cough and Congestion Cherry 100 mg/5mL; 5 mg/5mL 55758-0013-04 Pharmadel 1 bottle — — FDA listed —
SanaTos Mucus Relief Cold Toddlers 50 mg/2.5mL; 2.5 mg/2.5mL 55758-0307-02 Pharmadel 59 ml — — FDA listed —
Mucus Relief DM Max 20 mg/20mL; 400 mg/20mL 55910-0146-95 DOLGENCORP, 266 ml — — FDA listed —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 55910-0505-08 Dolgencorp, 266 ml — — FDA listed —
rexall dm cough and congestion relief 20 mg/20mL; 400 mg/20mL 55910-0755-26 Dolgencorp, 1 bottle — — FDA listed —
GeriCare Tussin DM Max 20 mg/20mL; 400 mg/20mL 57896-0591-08 GERI-CARE 237 ml — — FDA listed —
Mucinex Fast-Max DM Max 20 mg/20mL; 400 mg/20mL 63824-0019-22 Reckitt 2 bottles — — Discontinued —
Mucus Relief DM Max Maximum Strength 20 mg/20mL; 400 mg/20mL 63868-0235-06 QUALITY 177 ml — — Discontinued —
Childrens Mucus and Cough Relief 5 mg/5mL; 100 mg/5mL 63868-0771-04 Chain 1 bottle — — FDA listed —
DM Max 20 mg/20mL; 400 mg/20mL 63941-0518-25 Best 177 ml — — FDA listed —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 67091-0342-06 WINCO 180 ml — — FDA listed —
Premier Value Maximum Strength 20 mg/20mL; 400 mg/20mL 68016-0740-04 PHARMACY 1 bottle — — FDA listed —
Mucus Relief DM Honey and Berry Flavor 20 mg/20mL; 400 mg/20mL 68163-0605-06 RARITAN 180 ml — — FDA listed —
berkley and jensen tussin dm 20 mg/20mL; 400 mg/20mL 68391-0299-34 BJWC 1 bottle — — FDA listed —
Berkley and Jensen Tussin DM Max 20 mg/20mL; 400 mg/20mL 68391-0711-34 BJWC 1 bottle — — FDA listed —
Mucus Relief DM Max Maximum Strength 20 mg/20mL; 400 mg/20mL 69256-0505-06 Harris 177 ml — — FDA listed —
Tussin DMMax 20 mg/20mL; 400 mg/20mL 69618-0072-58 RELIABLE 1 bottle — — FDA listed —
Kids Cough and Chest Congestion 100 mg/5mL; 5 mg/5mL 69676-0037-09 Genexa 1 bottle — — FDA listed —
CVS Childrens Cough Relief 5 mg/5mL; 100 mg/5mL 69842-0577-04 CVS 1 bottle — — FDA listed —
tussin dm 20 mg/20mL; 400 mg/20mL 69842-0819-26 CVS 1 bottle — — FDA listed —
Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 69842-0904-06 CVS 177 ml — — FDA listed —
Cough and Chest Congestion DM Adult 20 mg/20mL; 400 mg/20mL 69842-0926-06 CVS 177 ml — — FDA listed —
CVS Mucus Relief DM Maximum Strength 20 mg/20mL; 400 mg/20mL 69842-0937-06 CVS 180 ml — — FDA listed —
Childrens Mucus and Cough Relief 5 mg/5mL; 100 mg/5mL 70000-0630-01 CARDINAL 1 bottle — — FDA listed —
basic care tussin dm max 20 mg/20mL; 400 mg/20mL 72288-0293-34 Amazon.com 1 bottle — — FDA listed —
Mucinex Fast-Max Kickstart Severe Congestion and Cough Maximum Strength 400 mg/1; 20 mg 72854-0159-66 Reckitt 180 liquids — — FDA listed —
Dr Kids Cough and Chest Congestion 100 mg/5mL; 5 mg/5mL 73282-2523-02 CalmCo 18 vials — — FDA listed —
Childrens Mucus Relief Cough Cherry Liquid 5 mg/5mL; 100 mg/5mL 76162-0294-04 Topco 1 bottle — — FDA listed —
Maximum Strength Mucus Relief DM Max 20 mg/20mL; 400 mg/20mL 76162-0628-58 Topco 177 ml — — FDA listed —
TOPCO Childrens Cough Relief 5 mg/5mL; 100 mg/5mL 76162-0751-04 Topco 1 bottle — — FDA listed —
Childrens Mucus Relief Cough - Cherry Flavor 5 mg/5mL; 100 mg/5mL 76281-0512-24 AptaPharma 1 bottle — — FDA listed —
Target Childrens Cough Relief 5 mg/5mL; 100 mg/5mL 82442-0751-04 TARGET 1 bottle — — FDA listed —
Mucus Relief Cough and Congestion Childrens 5 mg/5mL; 100 mg/5mL 82673-0102-04 KinderFarms, 1 bottle — — FDA listed —
AXIM DM Max 20 mg/20mL; 400 mg/20mL 82706-0013-01 VIVUNT 177 ml — — FDA listed —
AXIV DM Max 20 mg/20mL; 400 mg/20mL 82706-0024-01 VIVUNT 177 ml — — FDA listed —
Mucus Relief DM 20 mg/20mL; 400 mg/20mL 83324-0323-06 Chain 177 ml — — FDA listed —
Tussin DM 20 mg/20mL; 400 mg/20mL 83324-0324-04 Chain 1 bottle — — FDA listed —
Dr. Simi Children s Cough 5 mg/5mL; 100 mg/5mL 85786-0604-04 Farmacias 1 bottle — — FDA listed —
Target Cough plus Chest Congestion DM Max with Honey 20 mg/20mL; 400 mg/20mL 11673-0775-08 TARGET 1 bottle — — 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

🏛️
2018
On the market since
Sep 2018
📍
2026
Currently FDA-listed
8 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 Red
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.

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.

Manufacturer & labeler

LabelerAmerican Sales Company
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code41520
First marketedSep 2018
Product typeHuman Otc Drug
Portfolio100 products on file

More NDCs from American Sales Company labeler code 41520

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

⏱️ Dosage and Administration 67 words ▾

Directions • do not take more than 6 doses in any 24-hour period • measure only with dosing cup provided • keep dosing cup with product • mL = milliliter • this adult product is not intended for use in children under 12 years of age age dose adults and children 12 years and over 20 mL every 4 hours children under 12 years do not use

⚠️ Warnings 158 words ▾

Warnings Do not use 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 • cough that occurs with too much phlegm (mucus) • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema Stop use and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.

A persistent cough may be a sign 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 (1-800-222-1222).

📦 Storage and Handling 18 words ▾

Other information • each 20 mL contains: sodium 13 mg • store at 20-25°C (68-77°F). Do not refrigerate.

🧪 Active Ingredient 15 words ▾

Active ingredients (in each 20 mL) Dextromethorphan HBr, USP 20 mg Guaifenesin, USP 400 mg

🧪 Inactive Ingredients 35 words ▾

Inactive ingredients acetic acid, anhydrous citric acid, carboxymethylcellulose sodium, FD&C blue no. 1, FD&C red no. 40, flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose, xanthan gum

🎯 Purpose 4 words ▾

Purposes Cough suppressant Expectorant

📄 Do Not Use 55 words ▾

Do not use 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 34 words ▾

Ask a doctor before use if you have • cough that occurs with too much phlegm (mucus) • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

📄 Stop Use and Ask a Doctor If 36 words ▾

Stop use and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 22 words ▾

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).

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-719-9260

📄 Package Label / Principal Display Panel 72 words ▾

Package/Label Principal Display Panel CAREone ® Compare to the active ingredients in Robitussin® Maximum Strength Cough + Chest Congestion DM TUSSIN DM COUGH + CHEST CONGESTION Cough Suppressant-Dextromethorphan HBr Expectorant-Guaifenesin Maximum Strength Relieves: • Cough • Mucus Adult For Ages 12 & Over Non-Drowsy Alcohol Free Gluten Free Same Effective Cough Relief* *Compared to our previous (10 mL) formula Raspberry & Menthol Flavor OUR PHARMACISTS RECOMMEND 4 FL OZ (118 mL) 2b7-of-tussin-dm.jpg

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

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 careone tussin dm (this brand).

Top reported reactions

Blister1
Clonus1
Dehydration1
Dermatitis1
Diarrhoea1
Drug Abuse1
Dry Skin1

Age at onset

Adult1

Reporter sex

6 reports
Male · 80%
Female · 20%

Serious outcomes

Hospitalization3
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 1 0
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.

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 ✓ Available
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.
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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 bottle (41520-0931-26). 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?
American Sales Company 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.
← 41520-0929-30 · FOODHOLD 41520-0938-50 · FOODHOLD →
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.