NDC 47682-0735-33 — Medique at Home Decorel Forte Acetaminophen

🆔 Identity & classification

FDA NDC (as labeled) 47682-735-33

Product NDC 47682-735

11-digit billing NDC 47682073533

RxCUI 1098435

UNII 495W7451VQ, 9D2RTI9KYH, 04JA59TNSJ, 362O9ITL9D

Application # M012

SPL Set ID e648f017-9e30-df6c-e053-2995a90adcd0

Established class (EPC) Expectorant

Physiologic effect Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2022-09-26

Route ORAL

Dosage form TABLET, FILM COATED

Substance GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN

Why two NDCs? The FDA registers this code as 47682-735-33 — 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 → 47682-0735-33. Same drug, same package — only the format differs.

Where does this data come from?

Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Anilides class.

Drug family (ATC) Anilides

Where does this data come from?

Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerUnifirst First Aid Corporation

FDA applicationM012 (OTC MONOGRAPH DRUG)

Labeler code47682

First marketedSep 2022

Product typeHuman Otc Drug

Portfolio183 products on file

🔎 All NDCs from Unifirst First Aid Corporation

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

📖 About the active ingredient MedlinePlus · NLM

General information about the ingredient itself — the description of this specific product follows below.

Acetaminophen is used to relieve mild to moderate pain and to reduce fever. Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Read the full MedlinePlus article ↗

🧪 What is this product?

Medique at Home Decorel Forte is an oral film-coated tablet that is an over-the-counter cold and cough product marketed under FDA's OTC monograph rules. It contains four active ingredients: acetaminophen, typically used to reduce fever and relieve minor aches and pain; dextromethorphan, commonly used as a cough suppressant; guaifenesin, an expectorant typically used to help thin mucus and make coughs more productive; and phenylephrine, a nasal decongestant typically used to relieve sinus and nasal congestion. This combination is meant to address multiple cold and flu symptoms at once.

Patient education

📘 MedlinePlus patient leaflet ↗

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 orange

ShapeCapsule

Imprint44;546

Size17 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.

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: 2 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
Physicians Care Non-Drowsy Cold and Cough 325 mg/1; 10 mg/1; 5 mg/1; 100 mg 00924-0142-01	Acme	2 tablets	—	—	FDA listed	—
Head Congestion and Flu Severe Relief 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 11822-5462-09	Rite	10 tablets	—	—	FDA listed	—
Sedalmex XL Flu 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 27854-0350-01	Belmora	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 36800-0474-02	TOPCO	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 37808-0574-02	HEB	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 41163-0713-02	United	12 tablets	—	—	FDA listed	—
head congestion plus flu severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 41250-0574-02	MEIJER	12 tablets	—	—	Discontinued	—
Multi-Symptom Cold Relief 10 mg/1; 100 mg/1; 325 mg/1; 5 mg 47682-0047-80	Unifirst	2 tablets	—	—	FDA listed	—
Medique Decorel Forte 5 mg/1; 325 mg/1; 10 mg/1; 100 mg 47682-0435-36	Unifirst	2 tablets	—	—	FDA listed	—
Medique at Home Decorel Forte 100 mg/1; 10 mg/1; 5 mg/1; 325 mgthis 47682-0735-33	Unifirst	2 tablets	—	—	FDA listed	—
Medi-First Cough Cold 5 mg/1; 325 mg/1; 10 mg/1; 100 mg 47682-0835-36	Unifirst	2 tablets	—	—	FDA listed	—
Medi-First Plus Cough Cold 100 mg/1; 5 mg/1; 325 mg/1; 10 mg 47682-0836-36	Unifirst	2 tablets	—	—	FDA listed	—
CETAFEN COUGH and COLD 100 mg/1; 5 mg/1; 325 mg/1; 10 mg 50332-0141-03	HART	2 tablets	—	—	FDA listed	—
SUDAFED PE Head Congestion Plus Flu Severe 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 50580-0450-01	Kenvue	12 tablets	—	—	FDA listed	—
Head Congestion Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 50804-0274-02	GOODSENSE	12 tablets	—	—	FDA listed	—
Sinus PE Head Congestion and Flu Severe 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 51316-0546-08	CVS	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 53943-0274-02	DISCOUNT	12 tablets	—	—	FDA listed	—
Head Congestion Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 63868-0102-24	CHAIN	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 63941-0274-02	VALU	12 tablets	—	—	FDA listed	—
Head Congestion plus Flu Severe PE 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 72036-0274-02	HARRIS	12 tablets	—	—	FDA listed	—
Head Congestion Plus Flu Severe Pe 325 mg/1; 10 mg/1; 100 mg/1; 5 mg 72476-0174-02	RETAIL	12 tablets	—	—	FDA listed	—
Thompson Cough and Cold Multi-Symptom Relief 100 mg/1; 5 mg/1; 325 mg/1; 10 mg 73408-0835-80	Thompson	2 tablets	—	—	FDA listed	—
Cold Terminator Cold Relief 5 mg/1; 325 mg/1; 10 mg/1; 100 mg 84269-2556-01	Wildman	2 tablets	—	—	FDA listed	—
Medique at Home Decorel Forte 100 mg/1; 10 mg/1; 5 mg/1; 325 mg 85766-0174-01	Sportpharm	2 tablets	—	—	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

🏛️

2022

On the market since

Sep 2022

📍

2026

Currently FDA-listed

4 years listed

🔒

·

No generic listed yet

brand only

ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?

Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
47682-0735-33 You're viewing this	50 PACKET in 1 BOX (47682-735-33) / 2 TABLET, FILM COATED in 1 PACKET	2022-09-26	Active
47682-0735-99	2 TABLET, FILM COATED in 1 PACKET (47682-735-99)	2022-09-26	Active

Pack size FAQ

What quantity is in NDC 47682-0735-33?

NDC 47682-0735-33 is listed by the FDA — 50 packet in 1 box / 2 tablet, film coated in 1 packet.

What NDC number is used to bill for this package of Medique at Home Decorel Forte Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride 100 mg; 10 mg; 5 mg; 325 mg Tablet, Film Coated?

Bill NDC 47682-0735-33 — the 11-digit billing format is 47682073533. 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

What data is (and isn’t) available for this NDC — tap to expand

NDC identity (package / product / labeler codes)	✓ Available
Labeler	✓ Available
Product & package description	✓ Available
Marketing category & status	✓ Available
Active ingredient / dosage form / route	✓ Available
FDA label (SPL via DailyMed)	✓ Available
Package photos	— Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured)	— Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS)	— Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data	— Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk	— Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD)	— Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.

“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?

An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.

Why is there no price listed?

The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.

Is the NDC printed on the package the same as the 11-digit billing NDC?

Yes, they identify this exact package in different formats. The FDA registers it as 47682-735-33, 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: 47682-0735-33, written without dashes as 47682073533. 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 47682-0735-33, the first segment (47682) is the labeler code FDA assigned to Unifirst First Aid Corporation; the middle segment (0735) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (33) 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 Unifirst First Aid Corporation. Listing status can change — the directory data on this page refreshes weekly.

Does this product come in other package sizes?

Yes — the FDA directory lists 1 other package presentation of this same product, including 2 tablets (47682-0735-99). 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?

Unifirst First Aid Corporation 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 44 words ▾

Uses Temporarily relieves these symptoms due to the common cold: headache nasal congestion cough minor aches and pains sore throat sinus congestion and pressure helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive Temporarily reduces fever.

⏱️ Dosage and Administration 37 words ▾

Directions do not take more than directed Adults and children: (12 years and over): take 2 caplets every 4 hours not to take more than 10 caplets in 24 hours Children under 12 years: ask a doctor

⚠️ Warnings 97 words ▾

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: blisters rash skin reddening If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

🧪 Active Ingredient 19 words ▾

Active ingredients (in each caplet) Acetaminophen 325 mg Dextromethorphan HBr 10 mg Guaifenesin 100 mg Phenylephrine HCl 5 mg

🧪 Inactive Ingredients 30 words ▾

Inactive ingredients corn starch, crospovidone, FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, silicon dioxide, sodium starch glycolate, stearic acid, talc, titanium dioxide

🎯 Purpose 9 words ▾

Purpose Pain reliever/fever reducer Cough suppressant Expectorant Nasal decongestant

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

🔗 Related NDC lookups

🧪 All Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride NDCsSame ingredient 🏭 All Unifirst labeler NDCsLabeler code 47682 📚 All Expectorant NDCsDrug class