Home › NDC Lookup › Ingredients › Acetaminophen, Dextromethorphan Hydrobro... › 11822-4099-00
severe cold and flu relief acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL Solution, 355 mL — NDC 11822-4099-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

severe cold and flu relief acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL Solution, 355 mL — NDC 11822-4099-0 (Billing 11822-4099-00)

by Rite Aid Corporation · 355 mL in 1 BOTTLE

This is a package of 355 mL of severe cold and flu relief acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL Solution from Rite Aid Corporation, marketed since Jun 2023 and currently FDA-listed, this package's marketing is listed to end Oct 2026. It is this product's only package size.

NDC 11822-4099-00
🏷️ FDA NDC (as labeled) 11822-4099-0 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11822-4099-0
Product NDC 11822-4099
11-digit billing NDC 11822409900
RxCUI 1431245
UNII 362O9ITL9D, 9D2RTI9KYH, V9BI9B5YI2, 04JA59TNSJ
Application # M012
SPL Set ID 4b8ae971-ab57-4937-a878-72d905d7b849
Established class (EPC) Antihistamine; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; Uncompetitive NMDA Receptor Antagonists [MoA
Mechanism of action Adrenergic alpha1-Agonists; Histamine Receptor Antagonists; Sigma-1 Receptor Agonists
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-06-30
Marketing end 2026-10-31
Route ORAL
Dosage form SOLUTION
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Quick answers
  • RxCUI (RxNorm): 1431245
Why two NDCs? The FDA registers this code as 11822-4099-0 — 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 → 11822-4099-00. 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 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.

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?

This is an oral liquid solution marketed as a severe cold and flu relief product under FDA's over-the-counter monograph rules. It contains acetaminophen, a pain reliever and fever reducer; dextromethorphan, a cough suppressant; doxylamine succinate, a sedating antihistamine typically used to promote sleep; and phenylephrine hydrochloride, a decongestant. The combination is formulated to address multiple cold and flu symptoms in a single dose.

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.

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.
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
11822-4099-00 You're viewing this Main listing 355 mL in 1 BOTTLE 2023-06-30 Oct 31, 2026 Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense Severe NightTime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00113-0019-40 L. 354 ml $0.010 — Availability likely —
foster and thrive nighttime severe cold and flu relief 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 70677-1030-01 Strategic 355 ml $0.013 — FDA listed —
Good Sense Severe NightTime Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00113-0763-34 L. 237 ml — — Discontinued —
good sense night time cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 00113-2501-40 L. 354 ml — — FDA listed —
Night Time Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00363-0331-26 Walgreen 237 ml — — FDA listed —
severe cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00363-0623-40 Walgreen 355 ml — — FDA listed —
Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00363-0763-40 Walgreen 355 ml — — FDA listed —
nighttime severe cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 00363-2029-40 Walgreen 355 ml — — FDA listed —
Walgreen NightTime Cold and Flu relief 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 00363-6142-12 WALGREENS 354 ml — — FDA listed —
Nighttime Severe Honey Cold and Flu 6.25 mg/15mL; 325 mg/15mL; 10 mg/15mL; 5 mg/15mL 11673-0322-01 TARGET 354 ml — — FDA listed —
Nighttime severe cold and flu 20 mg/30mL; 650 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 11673-0828-01 TARGET 354 ml — — FDA listed —
nighttime severe cold and flu relief 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 11822-0511-01 Rite 355 ml — — FDA listed —
severe cold and flu relief 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 11822-0763-01 Rite 355 ml — — FDA listed —
severe cold and flu relief 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mLthis 11822-4099-00 Rite 355 ml — — FDA listed —
Signature Care Nighttime Severe Cold and Flu Relief 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 21130-0129-40 Safeway 355 ml — — FDA listed —
NightTime Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 30142-0763-40 Kroger 354 ml — — FDA listed —
topcare nite time cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 36800-0291-40 Topco 355 ml — — FDA listed —
Vicks NyQuil Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 37000-0812-01 The 30 ml — — FDA listed —
Vicks NyQuil Severe Cold and Flu 10 mg/30mL; 12.5 mg/30mL; 20 mg/30mL; 650 mg/30mL 37000-0815-08 The 236 ml — — FDA listed —
nighttime severe cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 37808-0763-40 H 355 ml — — FDA listed —
equaline nighttime severe cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 41163-0763-40 United 355 ml — — FDA listed —
Severe Cold and Flu Nighttime Honey 10 mg/15mL; 5 mg/15mL; 6.25 mg/15mL; 325 mg/15mL 41226-0767-01 Kroger 354 ml — — FDA listed —
Nighttime Severe Cold and Flu 12.5 mg/30mL; 10 mg/30mL; 650 mg/30mL; 20 mg/30mL 41226-0775-01 Kroger 354 ml — — FDA listed —
Nitetime Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 41250-0763-40 Meijer 355 ml — — FDA listed —
nitetime cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 41250-0811-40 Meijer 355 ml — — FDA listed —
CareOne Nighttime Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 41520-0561-40 American 355 ml — — FDA listed —
Severe Cold and Flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 42507-0020-40 HyVee 355 ml — — FDA listed —
Severe Cold and Flu Night time 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 42507-0763-40 HyVee 355 ml — — FDA listed —
severe cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 42507-0861-40 HyVee 355 ml — — FDA listed —
equate nighttime cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 49035-0807-40 Wal-Mart 355 ml — — FDA listed —
Severe cold and flu Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 49580-0416-08 P 237 ml — — FDA listed —
Severe cold and flu Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 49580-4160-08 P 237 ml — — FDA listed —
Tylenol Cold plus Flu plus Cough Night 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 50580-0369-01 Kenvue 240 ml — — FDA listed —
nighttime severe 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 51316-0179-40 CVS 355 ml — — FDA listed —
Severe Cold And Flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 51316-0533-40 CVS 355 ml — — FDA listed —
CVS NightTime Cold 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 51316-0641-12 CVS 354 ml — — FDA listed —
Severe Nighttime Cold and Flu Relief 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 55319-0641-08 Family 237 ml — — FDA listed —
Severe cold and flu Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 55910-0716-08 Dolgencorp, 237 ml — — FDA listed —
dg health cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 55910-0900-34 Dolgencorp, 237 ml — — FDA listed —
DG Health Cold and Flu Severe 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 55910-0928-40 Dolgencorp 355 ml — — FDA listed —
nitetime severe 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 56062-0763-40 Publix 355 ml — — FDA listed —
Rompe Pecho Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 58593-0830-06 EFFICIENT 1 bottle — — FDA listed —
Nighttime SEVERE 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 59640-0423-40 H 355 ml — — FDA listed —
Severe Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 59779-0763-34 CVS 237 ml — — Discontinued —
VICKS NyQuil SEVERE HONEY FLAVOR COLD and FLU 325 mg/15mL; 5 mg/15mL; 10 mg/15mL; 6.25 mg/15mL 69423-0807-08 Procter 236 ml — — FDA listed —
Vicks NyQuil Severe Honey Cold and Flu 325 mg/15mL; 5 mg/15mL; 10 mg/15mL; 6.25 mg/15mL 69423-0968-08 Procter 236 ml — — FDA listed —
NyQuil VapoCOOL SEVERE COLD and FLU plus CONGESTION 10 mg/30mL; 12.5 mg/30mL; 20 mg/30mL; 650 mg/30mL 69423-0989-08 The 236 ml — — FDA listed —
Nighttime Severe 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 69842-0800-40 CVS 355 ml — — FDA listed —
basic care nighttime severe cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 72288-0189-40 Amazon.com 355 ml — — FDA listed —
basic care nighttime severe cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 72288-0601-40 Amazon.com 355 ml — — FDA listed —
basic care nighttime severe cold and flu 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 72288-0639-40 Amazon.com 355 ml — — FDA listed —
topcare nite time cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 76162-0202-40 Topco 355 ml — — FDA listed —
night time cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 79481-8999-00 Meijer, 355 ml — — FDA listed —
equate nighttime cold and flu 325 mg/15mL; 10 mg/15mL; 6.25 mg/15mL; 5 mg/15mL 79903-0122-12 WALMART 1 bottle — — FDA listed —
Cold and Flu plus Congestion Nighttime 650 mg/30mL; 20 mg/30mL; 12.5 mg/30mL; 10 mg/30mL 79903-0191-12 WALMART 355 ml — — FDA listed —
Nighttime Severe Cold and Flu 12.5 mg/30mL; 10 mg/30mL; 650 mg/30mL; 20 mg/30mL 85828-0775-01 Grocery 354 ml — — 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

🏛️
2023
On the market since
Jun 2023
📍
2026
Currently FDA-listed
3 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.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

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

  • UNII XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII 35SW5USQ3G
    A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
  • UNII 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 3P3ONR6O1S
    A synthetic green dye approved by the FDA for use in medicines and foods. It serves as a colorant to make the pill or liquid visually distinctive and help with product identification.
  • UNII WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • 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.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 3WJQ0SDW1A
    Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
  • 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 SB8ZUX40TY
    Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • UNII 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
  • 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 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.

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

The official label also statesanhydrous citric acid, D&C yellow #10, edetate disodium, FD&C green #3, FD&C red #40, FD&C yellow #6, flavor, glycerin, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol solution, sucralose, 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.

Manufacturer & labeler

LabelerRite Aid Corporation
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code11822
First marketedJun 2023
Product typeHuman Otc Drug
Portfolio326 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.

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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 66 words ▾

Uses temporarily relieves common cold/flu symptoms: • nasal congestion • sinus congestion and pressure • cough due to minor throat and bronchial irritation • cough to help you sleep • minor aches and pains • headache • sore throat • fever • runny nose and sneezing • reduces swelling of nasal passages • temporarily restores freer breathing through the nose • promotes nasal and/or sinus drainage

⏱️ Dosage and Administration 65 words ▾

Directions • take only as directed – see Overdose warning • only use the dose cup provided • do not exceed 4 doses per 24 hrs adults & children 12 yrs & over 30 mL every 4 hrs children 6 to under 12 yrs 15 mL every 4 hrs children 4 to under 6 yrs ask a doctor children under 4 yrs do not use

⚠️ Warnings ~2 min read ▾

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if • adult takes more than 4,000 mg of acetaminophen in 24 hours • child takes more than 5 doses in 24 hours • taken with other drugs containing acetaminophen • adult has 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: • skin reddening • blisters • rash 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. Do not use • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. • 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. • if you have ever had an allergic reaction to this product or any of its ingredients • to make a child sleepy Ask a doctor before use if you have • liver disease • heart disease • high blood pressure • glaucoma • thyroid disease • diabetes • cough that occurs with too much phlegm (mucus) • trouble urinating due to an enlarged prostate gland • a breathing problem such as emphysema or chronic bronchitis • persistent or chronic cough such as occurs with smoking, asthma, or emphysema Ask a doctor or pharmacist before use if you are • taking the blood thinning drug warfarin • taking sedatives or tranquilizers When using this product • do not use more than directed • excitability may occur, especially in children • marked drowsiness may occur • avoid alcoholic drinks • be careful when driving a motor vehicle or operating machinery • alcohol, sedatives, and tranquilizers may increase drowsiness Stop use and ask a doctor if • you get nervous, dizzy or sleepless • pain, nasal congestion, or cough gets worse or lasts more than 5 days (children) or 7 days (adults) • fever gets worse or lasts more than 3 days • redness or swelling is present • new symptoms occur • cough comes back or occurs with 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.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

🧪 Active Ingredient 21 words ▾

Active ingredients (in each 15 mL) Acetaminophen 325 mg Dextromethorphan HBr 10 mg Doxylamine Succinate 6.25 mg Phenylephrine HCl 5 mg

🧪 Inactive Ingredients 40 words ▾

Inactive ingredients anhydrous citric acid, D&C yellow #10, edetate disodium, FD&C green #3, FD&C red #40, FD&C yellow #6, flavor, glycerin, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol solution, sucralose, xanthan gum

🎯 Purpose 9 words ▾

Purpose Pain reliever/fever reducer Cough suppressant Antihistamine Nasal decongestant

📄 Do Not Use 104 words ▾

Do not use • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. • 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. • if you have ever had an allergic reaction to this product or any of its ingredients • to make a child sleepy

📄 Ask a Doctor Before Use If 66 words ▾

Ask a doctor before use if you have • liver disease • heart disease • high blood pressure • glaucoma • thyroid disease • diabetes • cough that occurs with too much phlegm (mucus) • trouble urinating due to an enlarged prostate gland • a breathing problem such as emphysema or chronic bronchitis • persistent or chronic cough such as occurs with smoking, asthma, or emphysema

📄 Ask a Doctor or Pharmacist Before Use If 22 words ▾

Ask a doctor or pharmacist before use if you are • taking the blood thinning drug warfarin • taking sedatives or tranquilizers

📄 When Using This Product 46 words ▾

When using this product • do not use more than directed • excitability may occur, especially in children • marked drowsiness may occur • avoid alcoholic drinks • be careful when driving a motor vehicle or operating machinery • alcohol, sedatives, and tranquilizers may increase drowsiness

📄 Stop Use and Ask a Doctor If 73 words ▾

Stop use and ask a doctor if • you get nervous, dizzy or sleepless • pain, nasal congestion, or cough gets worse or lasts more than 5 days (children) or 7 days (adults) • fever gets worse or lasts more than 3 days • redness or swelling is present • new symptoms occur • cough comes back or occurs with rash or headache that lasts. These could be signs 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 46 words ▾

Keep out of reach of children. Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

📄 Other Information 15 words ▾

Other information • each 15 mL contains: sodium 15 mg • store at 20-25°C (68-77°F)

📄 Questions or Comments 2 words ▾

Questions? 1-800-719-9260

📄 Package Label / Principal Display Panel 59 words ▾

Package/Label Principal Display Panel Compare to the active ingredients of Vicks ® NyQuil ® Severe Honey Flavor FREE FROM | GLUTEN FREE MAXIMUM STRENGTH SEVERE COLD & FLU RELIEF NIGHTTIME ACETAMINOPHEN PHENYLEPHRINE HCl DEXTROMETHORPHAN HBr DOXYLAMINE SUCCINATE PAIN RELIEVER / FEVER REDUCER NASAL DECONGESTANT COUGH SUPPRESSANT ANITHISTAMINE HONEY FLAVOR 12 FL OZ (355 mL) severe cold and flu relief-image

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 Acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride — the ingredient across all brands.

Top reported reactions

Choking13
Foreign Body In Throat8
Dizziness4
Vomiting4
Dyspnoea3
Oropharyngeal Pain3
Product Use Complaint3

Age at onset

Adult9
Elderly5

Reporter sex

34 reports
Male · 12%
Female · 88%
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 4 1
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
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

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 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.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page it is currently marketed — but Rite Aid Corporation has reported a marketing end date of 2026-10-31, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
Rite 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.
← 11822-4040-01 · Rite 11822-4130-02 · Rite →
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.