DELSYM Dextromethorphan 30 mg/5mL Suspension, Extended Release
by A-S Medication Solutions · 1 BOTTLE in 1 CARTON (50090-0224-0) / 89 mL in 1 BOTTLE
NDC 50090-0224-00
🏷️ FDA NDC (as labeled)
50090-0224-0
billing pads the package segment with a zero
OTC
Brand
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
50090-0224-0
Product NDC
50090-0224
11-digit billing NDC
50090022400
NCPDP billing unit
ML — per mL (volume)
UNII
7355X3ROTS
Application #
NDA018658
SPL Set ID
2ac3cac7-5980-4ff5-9939-d494c3daa9d2
Established class (EPC)
Uncompetitive N-methyl-D-aspartate Receptor Antagonist; Sigma-1 Agonist
Mechanism of action
Uncompetitive NMDA Receptor Antagonists; Sigma-1 Receptor Agonists
DEA schedule
Non-controlled
Marketing category
NDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2010-05-04
Route
ORAL
Dosage form
SUSPENSION, EXTENDED RELEASE
Substance
DEXTROMETHORPHAN
GPI-14
4310203060G110
GPI class
Delsym
GCN Seq No
004630
GCN
17802
HICL code
010295
Ingredient (HICL)
Dextromethorphan Polistirex
HIC1 code
H
Therapeutic class — broad (HIC1)
Nervous System (Except Autonomic)
HIC2 code
H6
Therapeutic class — intermediate (HIC2)
Drugs Acting Principally On The Midbrain
HIC3 code
H6C
Therapeutic class — specific (HIC3)
Antitussives, Non-Opioid
AHFS code
48:08.00.00
AHFS class
Antitussives
FDB label name
DELSYM 30 MG/5 ML SUSPENSION
FDB brand name
Delsym
Legend status
O — Over-the-counter (OTC) drug or device
Why two NDCs?
The FDA registers this code as 50090-0224-0 — a 5-4-1 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 package segment → 50090-0224-00. 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
LabelerA-S Medication Solutions
Application holderRECKITT BENCKISER LLC
FDA applicationNDA018658 (NDA)
Labeler code50090
First marketedMay 2010
Product typeHuman Otc Drug
Portfolio2,781 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 DELSYM 30 MG/5 ML SUSPENSION Ingredient Dextromethorphan Polistirex
📖 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 won't necessarily silence your cough entirely, but it does temporarily suppress the cough reflex and reduce how intense and frequent your cough is. It can also help reduce that...
- What exactly does dextromethorphan do — will it stop my cough completely?
- It depends on your child's age and the specific product. Most dextromethorphan products should not be given to children under 4 years old without a doctor's guidance. Some products...
- This is a really important question. If your antidepressant is an MAOI (monoamine oxidase inhibitor), you absolutely cannot take dextromethorphan — not while you're on it, and not...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Dextromethorphan — tap one for details:
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 Dextromethorphan?
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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
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UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
-
UNII 2968PHW8QP
A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
-
UNII 7FLD91C86K
Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
-
UNII 7Z8S9VYZ4B
Ethylcellulose is a plant-derived thickener and film-former made by chemically modifying cellulose. It's used as a binder to hold tablet ingredients together, a coating to control how quickly medicine is released, or a thickener in liquid formulations.
-
UNII XY6UN3QB6S
A sweetener made from corn starch that contains fructose and glucose. It sweetens the medicine to improve taste and may help preserve the product.
-
UNII H77VEI93A8
A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
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UNII A2I8C7HI9T
Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
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UNII 6OZP39ZG8H
Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
-
UNII G2M7P15E5P
Polyethylene glycol 3350 is a synthetic polymer used as a solvent, humectant, and thickening agent in medicines. It helps dissolve other ingredients, retain moisture in the product, and achieve the desired consistency.
-
UNII 5H9W9GTW27
A synthetic polymer derived from styrene that binds and holds active ingredients together in solid forms. It's used as a binder and tablet/capsule filler to give the medicine its shape and help it stay intact.
-
UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII Z8IX2SC1OH
Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
-
UNII C151H8M554
A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
-
UNII 2944357O2O
A natural gum derived from the tragacanth shrub, used as a thickener, stabilizer, and binder in medicines. It helps create the right consistency and keeps ingredients evenly mixed throughout the product.
-
UNII TTV12P4NEE
Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
15 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescitric acid, edetate disodium, ethylcellulose, FD&C yellow no. 6, flavor, high fructose corn syrup, methylparaben, partially hydrogenated vegetable oil (soybean, cottonseed), polyethylene glycol 3350, polysorbate 80, propylene glycol, propylparaben, purified water, sucrose, tragacanth, xanthan gum
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 system | Per mL | 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.
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 |
|---|---|---|---|---|---|---|
| Good Sense Cough DM 30 mg/5mL 00113-0958-21 | L. | 1 bottle | $0.067 | — | Availability likely | — |
| cough dm 30 mg/5mL 00904-6312-56 | Major | 1 bottle | $0.067 | — | Availability likely | — |
| dextromethorphan polistirex extended release 30 mg/5mL 45802-0433-21 | Padagis | 1 bottle | $0.067 | — | Availability likely | — |
| Good Neighbor Pharmacy Cough DM ER 30 mg/5mL 46122-0141-21 | Amerisource | 1 bottle | $0.067 | — | Availability likely | — |
| Leader Cough DM 30 mg/5mL 70000-0187-01 | Cardinal | 1 bottle | $0.067 | — | Availability likely | — |
| leader childrens cough dm 30 mg/5mL 70000-0195-01 | Cardinal | 1 bottle | $0.067 | — | Availability likely | — |
| Leader Cough DM 30 mg/5mL 70000-0302-01 | Cardinal | 1 bottle | $0.067 | — | Availability likely | — |
| foster and thrive 12 hour cough relief 30 mg/5mL 70677-1025-01 | Strategic | 1 bottle | $0.067 | — | Availability likely | — |
| foster and thrive 12 hour cough relief 30 mg/5mL 70677-1026-01 | Strategic | 1 bottle | $0.067 | — | Availability likely | — |
| Delsym (Dextromethorphan) 30 mg/5mL 63824-0173-63 | Reckitt | 1 bottle | $0.102 | — | FDA listed | — |
| Delsym (Dextromethorphan) 30 mg/5mL 63824-0177-63 | Reckitt | 1 bottle | $0.102 | — | FDA listed | — |
| Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8655-10 | Haleon | 1 bottle | — | — | FDA listed | — |
| Childrens Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8725-10 | Haleon | 1 bottle | — | — | FDA listed | — |
| Childrens Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8726-10 | Haleon | 1 bottle | — | — | FDA listed | — |
| Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8753-03 | Haleon | 1 bottle | — | — | FDA listed | — |
| Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8754-15 | Haleon | 1 bottle | — | — | FDA listed | — |
| Robitussin 12 Hour Cough Relief 30 mg/5mL 00031-8755-15 | Haleon | 1 bottle | — | — | FDA listed | — |
| good sense cough dm 30 mg/5mL 00113-0384-21 | L. | 1 bottle | — | — | Discontinued | — |
| Cough DM 30 mg/5mL 00363-0384-21 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 00363-0494-21 | Walgreen | 1 bottle | — | — | Discontinued | — |
| childrens cough dm 30 mg/5mL 00363-0899-21 | Walgreen | 1 bottle | — | — | FDA listed | — |
| up and up 12 hour cough relief 30 mg/5mL 11673-0114-28 | Target | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 11822-0384-01 | Rite | 1 bottle | — | — | Discontinued | — |
| Cough DM 30 mg/5mL 11822-0494-01 | Rite | 1 bottle | — | — | Discontinued | — |
| Cough DM 30 mg/5mL 11822-0958-01 | Rite | 1 bottle | — | — | Discontinued | — |
| cough dm 30 mg/5mL 17856-6312-01 | ATLANTIC | 5 ml | — | — | FDA listed | — |
| signature care 12 hour cough relief 30 mg/5mL 21130-0012-21 | Safeway | 1 bottle | — | — | FDA listed | — |
| Signature Care Cough Relief 30 mg/5mL 21130-0520-21 | Safeway | 1 bottle | — | — | FDA listed | — |
| Cough Dm 30 mg/5mL 21130-0538-21 | Safeway | 1 bottle | — | — | FDA listed | — |
| signature care childrens 12 hour cough relief 30 mg/5mL 21130-0890-21 | Safeway | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 30142-0384-21 | Kroger | 1 bottle | — | — | FDA listed | — |
| cough dm 30 mg/5mL 30142-0494-21 | Kroger | 1 bottle | — | — | FDA listed | — |
| TopCare Cough DM 30 mg/5mL 36800-0494-21 | Topco | 1 bottle | — | — | FDA listed | — |
| Topcare Cough DM 30 mg/5mL 36800-0552-21 | Topco | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 37808-0384-21 | H | 1 bottle | — | — | FDA listed | — |
| equaline cough dm 30 mg/5mL 41163-0384-21 | United | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 41250-0384-28 | Meijer | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 41250-0494-28 | Meijer | 1 bottle | — | — | FDA listed | — |
| cough dm childrens 30 mg/5mL 41250-0899-28 | Meijer | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 41250-0958-28 | Meijer | 1 bottle | — | — | FDA listed | — |
| CareOne Cough DM 30 mg/5mL 41520-0384-21 | American | 1 bottle | — | — | FDA listed | — |
| CareOne Cough DM 30 mg/5mL 41520-0958-21 | American | 1 bottle | — | — | FDA listed | — |
| cough dm 30 mg/5mL 42507-0384-21 | HyVee | 1 bottle | — | — | FDA listed | — |
| cough dm 30 mg/5mL 42507-0494-21 | HyVee | 1 bottle | — | — | FDA listed | — |
| Equate Cough DM 30 mg/5mL 49035-0384-21 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| equate cough dm 30 mg/5mL 49035-0899-28 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Delsym 30 mg/5mLthis 50090-0224-00 | A-S | 1 bottle | — | — | FDA listed | — |
| 12 Hr Relief Cough Dm 30 mg/5mL 51316-0263-21 | CVS | 1 bottle | — | — | FDA listed | — |
| Childrens 12 Hr Cough Relief 30 mg/5mL 51316-0429-28 | CVS | 1 bottle | — | — | FDA listed | — |
| DG Health Cough DM 30 mg/5mL 55910-0384-21 | Dolgencorp | 1 bottle | — | — | FDA listed | — |
| DG Health Cough DM 30 mg/5mL 55910-0958-21 | Dolgencorp, | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 56062-0384-21 | Publix | 1 bottle | — | — | FDA listed | — |
| Dextromethorphan Polistirex 30 mg/5mL 58602-0610-05 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Dextromethorphan Polistirex 30 mg/5mL 58602-0611-05 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Dextromethorphan Polistirex 30 mg/5mL 58602-0617-05 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Dextromethorphan Polistirex 30 mg/5mL 58602-0618-05 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 59779-0384-21 | CVS | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 59779-0709-21 | CVS | 1 bottle | — | — | FDA listed | — |
| Cough DM 30 mg/5mL 59779-0958-21 | CVS | 1 bottle | — | — | FDA listed | — |
| Delsym 30 mg/5mL 63824-0171-22 | Reckitt | 1 cello | — | — | FDA listed | — |
| Delsym 30 mg/5mL 63824-0175-22 | Reckitt | 1 cello | — | — | FDA listed | — |
| Dextromethorphan Polistirex Extended-Release 30 mg/5mL 65162-0700-76 | Amneal | 1 bottle | — | — | FDA listed | — |
| Dextromethorphan Polistirex Extended-Release 30 mg/5mL 65162-0799-76 | Amneal | 1 bottle | — | — | FDA listed | — |
| dextromethorphan polistirex extended release 30 mg/5mL 72162-2281-02 | Bryant | 1 bottle | — | — | FDA listed | — |
| basic care cough dm 30 mg/5mL 72288-0384-28 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| basic care cough dm 30 mg/5mL 72288-0494-28 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| basic care childrens cough dm 30 mg/5mL 72288-0899-28 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| basic care childrens cough dm 30 mg/5mL 72288-0958-28 | Amazon.com | 1 bottle | — | — | 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
🏛️
2010
On the market since
May 2010
📍
2026
Currently FDA-listed
16 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.
🔬 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 DELSYM (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 42%
Female · 58%
Unknown · 0%
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 |
|---|---|---|---|
| 50090-0224-00 You're viewing this | 1 BOTTLE in 1 CARTON (50090-0224-0) / 89 mL in 1 BOTTLE | 2014-11-28 | 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 | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
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 50090-0224-0, 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: 50090-0224-00, written without dashes as 50090022400. 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 50090-0224-00, the first segment (50090) is the labeler code FDA assigned to A-S Medication Solutions; the middle segment (0224) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 A-S Medication Solutions. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
A-S Medication Solutions 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
📦 How Supplied / Storage and Handling
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the impulse to cough to help you get to sleep
⏱️ Dosage and Administration ▾
Directions shake bottle well before use measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor adults and children 12 years of age and over 10 mL every 12 hours, not to exceed 20 mL in 24 hours children 6 to under 12 years of age 5 mL every 12 hours, not to exceed 10 mL in 24 hours children 4 to under 6 years of age 2.5 mL every 12 hours, not to exceed 5 mL in 24 hours children under 4 years of age do not use
⚠️ Warnings ▾
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 chronic cough that lasts such as occurs with smoking, asthma, or emphysema cough that occurs with too much phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, 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.
📦 How Supplied / Storage and Handling ▾
HOW SUPPLIED Product: 50090-0224 NDC: 50090-0224-0 89 mL in a BOTTLE / 1 in a CARTON
📦 Storage and Handling ▾
Other information each 5 mL contains: sodium 7 mg store at 20-25°C (68-77°F) dosing cup provided
🧪 Active Ingredient ▾
Active ingredient (in each 5 mL) Dextromethorphan polistirex equivalent to 30 mg dextromethorphan hydrobromide
🧪 Inactive Ingredients ▾
Inactive ingredients citric acid, edetate disodium, ethylcellulose, FD&C yellow no. 6, flavor, high fructose corn syrup, methylparaben, partially hydrogenated vegetable oil (soybean, cottonseed), polyethylene glycol 3350, polysorbate 80, propylene glycol, propylparaben, purified water, sucrose, tragacanth, xanthan gum
🎯 Purpose ▾
Purpose Cough suppressant
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.