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Daytime Nighttime Cold Flu Relief Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl Kit — NDC 69842-896-24 (Billing 69842-0896-24)

by CVS Pharmacy · 1 KIT in 1 KIT * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 32 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE

This is a package of Daytime Nighttime Cold Flu Relief Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl Kit from CVS Pharmacy, marketed since Jul 2019 and currently FDA-listed, this package's marketing is listed to end Nov 2027. It is the main listing for this product, which comes in 2 package sizes.

NDC 69842-0896-24
🏷️ FDA NDC (as labeled) 69842-896-24 billing pads the product segment with a zero
This package
Contains1 capsule Pack sizes2 compare ↓
Main listing for product 69842-896 · Also comes in: 1 capsule 69842-896-48
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 6, 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) 69842-896-24
Product NDC 69842-896
11-digit billing NDC 69842089624
NCPDP billing unit EA — each (per item)
RxCUI 1086997, 1094549, 1426334, 2634564
Application # M012
SPL Set ID df6e522c-3e30-4aa0-8ab9-3b579c80bcad
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-07-31
Marketing end 2027-11-28
Dosage form KIT

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 065258
GCN 24902
HICL code 033966
Ingredient (HICL) Dm/Pe/Acetaminophen/Doxylamine
HIC1 code B
Therapeutic class — broad (HIC1) Respiratory System
HIC2 code B3
Therapeutic class — intermediate (HIC2) Drugs Affecting Primarily The Trachea And Bronchi
HIC3 code B3P
Therapeutic class — specific (HIC3) Non-Opioid Antitus-1Stgen Antihist-Decon-Analgesic
AHFS code 04:04.04.00
AHFS class Ethanolamine Derivatives
FDB label name CVS DAYTIME-NIGHTTIME COLD-FLU
FDB brand name Daytime-Nighttime Cold-Flu
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 065258
  • GCN: 24902
  • HICL (First Databank): 033966
  • AHFS class code: 04:04.04.00
  • RxCUI (RxNorm): 1086997
Why two NDCs? The FDA registers this code as 69842-896-24 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 69842-0896-24. 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

Label name CVS DAYTIME-NIGHTTIME COLD-FLU Ingredient Dm/Pe/Acetaminophen/Doxylamine
🧪 What is this product?

This is an over-the-counter combination cold and flu relief kit containing separate daytime and nighttime formulations. The daytime portion includes acetaminophen (a pain reliever and fever reducer) and phenylephrine (a decongestant), while the nighttime portion adds doxylamine succinate (an antihistamine that causes drowsiness) and dextromethorphan (a cough suppressant). This kit is marketed under FDA's OTC monograph rules for cold and flu symptom products.

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 eachPer 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: 1 capsule
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
69842-0896-24 You're viewing this Main listing 1 KIT in 1 KIT * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 32 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE 2019-07-31 Nov 28, 2027 Active
69842-0896-48 69842-896-48 1 KIT in 1 KIT * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 32 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE 2019-07-31 Nov 28, 2027 Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 kit in 1 kit * 16 blister pack in 1 carton / 1 capsule in 1 blister pack * 32 blister pack in 1 carton / 1 capsule in 1 blister pack * 8 blister pack in 1 carton / 1 capsule in 1 blister pack * 16 blister pack in 1 carton / 1 capsule.
What NDC number is used to bill for this package of Daytime Nighttime Cold Flu Relief Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl Kit?
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
foster and thrive daytime cold and flu relief nighttime cold and flu relief 70677-1028-01 Strategic 2 capsules $0.151 — FDA listed —
Goodnow cold flu day relief cold flu night relief 82501-1211-01 Gobrands, 2 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 41163-0901-48 United 1 capsule — — FDA listed —
NiteTime DayTime Cold and Flu 41250-0597-02 Meijer 1 kit — — FDA listed —
Daytime Nighttime Cold and Flu Relief Multi-Symptom 67091-0336-48 WinCo 16 capsules — — FDA listed —
Cold and Flu Day, Night 00363-1213-02 Walgreen 1 kit — — FDA listed —
daytime nighttime cold and flu 00363-1733-02 Walgreen 1 kit — — FDA listed —
Daytime Nighttime Cold Flu Relief 72476-0850-48 Care 16 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 11822-0851-04 Rite 8 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 21130-0058-48 Safeway, 16 capsules — — FDA listed —
equaline daytime and nighttime cold and flu relief 41163-0567-02 United 1 kit — — FDA listed —
equate daytime cold and flu nighttime cold and flu 49035-0718-02 Wal-Mart 1 kit — — FDA listed —
Cold and Flu Daytime, Nighttime, Multi-Symptom 00363-9012-48 Walgreens 8 capsules — — FDA listed —
Vicks DayQuil NyQuil ULTRA CONCENTRATED COLD and FLU 69423-0802-96 The 1 kit — — FDA listed —
Topcare Nite Time Day Time Cold and Flu 36800-0580-72 Topco 2 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 68016-0799-48 Chain 1 capsule — — Discontinued —
Cold And Flu Daytime-Nighttime 11673-0984-24 TARGET 8 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 49035-0192-48 EQUATE 16 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 69256-0901-48 Harris 1 capsule — — FDA listed —
basic care daytime nighttime cold and flu 72288-0733-02 Amazon.com 1 kit — — FDA listed —
Daytime Nighttime Cold Flu Relief 72476-0901-48 Care 32 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 55319-0566-24 Family 1 capsule — — FDA listed —
Daytime Nighttime Cold Flu Relief 67091-0393-48 WinCo 1 capsule — — FDA listed —
Severe Cold and Flu 00363-1597-02 Walgreen 1 kit — — FDA listed —
Cold and Flu Daytime, Nighttime, Multi-Symptom 00363-9011-24 Walgreens 8 capsules — — FDA listed —
Daytime Nighttime Cold Flu Relief 69842-0852-24 CVS 1 capsule — — FDA listed —
Daytime Nighttime Cold Flu Relief 81522-0901-48 FSA 1 capsule — — FDA listed —
Daytime Nighttime Cold Flu Relief 21130-0901-48 Safeway, 16 capsules — — FDA listed —
TopCare Day Time Nite Time Cold and Flu Relief 36800-0301-02 Topco 1 kit — — FDA listed —
Daytime Nighttime Cold and Flu Relief Multi-Symptom 59726-0901-24 P 8 capsules — — FDA listed —
daytime nighttime cold and flu 00363-0567-02 Walgreen 1 kit — — FDA listed —
Daytime Nighttime Cold Flu Reliefthis 69842-0896-24 CVS 1 capsule — — FDA listed —
basic care daytime cold and flu nighttime cold and flu 72288-0580-72 Amazon.com 2 capsules — — FDA listed —
Cold and Flu Daytime Nighttime 51316-0123-02 CVS 1 kit — — FDA listed —
Topcare Day Time Nite Time Cold and Flu 36800-0597-02 Topco 1 kit — — FDA listed —
Daytime Nighttime Cold Flu Relief 41163-0850-48 United 16 capsules — — FDA listed —
Daytime-Nighttime Severe Cold And Flu 41226-0627-24 KROGER 4 capsules — — FDA listed —
daytime nitetime cold and flu 41250-0733-02 Meijer 1 kit — — FDA listed —
dg health cold and flu relief 55910-0811-72 Dolgencorp 2 capsules — — FDA listed —
Severe Nighttime Severe Daytime 59779-0597-02 CVS 1 kit — — FDA listed —
Severe Cold and Flu Nighttime Daytime 42507-0597-02 HyVee 1 kit — — FDA listed —
Daytime Nighttime Cold And Flu 72288-0791-02 Amazon.com 1 kit — — FDA listed —
Good Sense Daytime Nighttime Cold And Flu 00113-5800-72 L. 2 capsules — — 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

🏛️
2019
On the market since
Jul 2019
📍
2026
Currently FDA-listed
7 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.

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

LabelerCVS Pharmacy
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code69842
First marketedJul 2019
Product typeHuman Otc Drug
Portfolio550 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

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 📄 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 58 words ▾

Uses DAYTIME temporarily relieves common cold and flu symptoms cough due to minor throat and bronchial irritation fever sore throat nasal congestion and sinus pressure headache minor aches and pain NIGHTTIME temporarily relieves common cold and flu symptoms cough due to minor throat and bronchial irritation sore throat headache minor aches and pains fever runny nose and sneezing

⏱️ Dosage and Administration 101 words ▾

Directions DAYTIME do not take more than directed (see Overdose warning) do not take more than 4 doses in 24 hours swallow whole; do not crush, chew, or dissolve adults and children 12 years and over; take 2 softgels with water every 4 hours. children under 12 years: do not use NIGHTTIME do not take more than directed (see Overdose warning) do not take more than 4 doses in 24 hours swallow whole; do not crush, chew, or dissolve adults and children 12 years and over: take 2 softgels with water every 6 hours children under 12 years: do not use

⚠️ Warnings ~2 min read ▾

Warnings DAYTIME NIGHTTIME Liver warning: These products contain 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 these products 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 DAYTIME NIGHTTIME 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.

Ask a doctor before use if you have DAYTIME liver disease heart disease diabetes thyroid disease high blood pressure cough that occurs with too much phlegm (mucus) trouble urinating due to an enlarged prostate gland persistent or chronic cough such as occurs with smoking, asthma, or emphysema NIGHTTIME liver disease glaucoma cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are DAYTIME taking the blood thinning drug warfarin NIGHTTIME taking the blood thinning drug warfarin taking sedatives or tranquilizers When using this product, DAYTIME do not exceed recommended dosage NIGHTTIME do not exceed recommended dosage excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if DAYTIME nervousness, dizziness or sleeplessness occur pain, cough, and nasal congestion gets worse or lasts more than 7 days redness or swelling is present new symptoms occur fever gets worse or lasts more than 3 days cough comes back or occurs with rash or headache that lasts.These could be signs of a serious condition.

NIGHTTIME pain or cough gets worse or lasts more than 7 days fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with rash headache that lasts. These could be a signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. Overdose warning : Taking more than the recommended dose can cause liver damage. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

📦 Storage and Handling 9 words ▾

Other information store between 15-30°C (59-86°F) avoid excessive heat

🧪 Active Ingredient 36 words ▾

Active ingredients for Daytime (in each softgel) Acetaminophen 325 mg Dextromethorphan HBr 10 mg Phenylephrine HCl 5 mg

Active ingredients for Nighttime (in each softgel) Acetaminophen 325 mg Dextromethorphan HBr 15 mg Doxylamine succinate 6.25 mg

🧪 Inactive Ingredients 52 words ▾

Inactive ingredients DAYTIME FD&C red #40, FD&C yellow #6, gelatin, glycerin, lecithin, light mineral oil, mannitol, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol, white ink NIGHTTIME D&C yellow #10, FD&C blue #1, gelatin, glycerin, lecithin, light mineral oil, mannitol, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol, white ink

🎯 Purpose 19 words ▾

Purpose for Daytime Pain reliever/fever reducer Cough suppressant Nasal decongestant

Purpose for Nighttime Pain reliever/fever reducer Cough suppressant Antihistamine

📄 Do Not Use 81 words ▾

Do not use DAYTIME NIGHTTIME 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.

📄 Ask a Doctor Before Use If 83 words ▾

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

📄 Ask a Doctor or Pharmacist Before Use If 28 words ▾

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

📄 When Using This Product 46 words ▾

When using this product, DAYTIME do not exceed recommended dosage NIGHTTIME do not exceed recommended dosage excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery

📄 Stop Use and Ask a Doctor If 109 words ▾

Stop use and ask a doctor if DAYTIME nervousness, dizziness or sleeplessness occur pain, cough, and nasal congestion gets worse or lasts more than 7 days redness or swelling is present new symptoms occur fever gets worse or lasts more than 3 days cough comes back or occurs with rash or headache that lasts.These could be signs of a serious condition. NIGHTTIME pain or cough gets worse or lasts more than 7 days fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with rash headache that lasts.

These could be a 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 57 words ▾

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

📄 Questions or Comments 8 words ▾

Questions or comments? Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

📄 Package Label / Principal Display Panel 185 words ▾

Principal Display Panel Compare to Vicks® DayQuil™ and NyQuil™ Cold & Flu LiquiCaps™active ingredients* DAYTIME COLD & FLU Acetaminophen Pain reliever; Fever reducer Dextromethorphan HBr Cough suppressant Phenylephrine HCI Nasal decongestant Multi-Symptom Relief Aches, Fever, Sore throat, Cough, Nasal congestion, Sinus Pressure SOFTGELS** NIGHTTIME COLD & FLU Acetaminophen Pain reliever; Fever reducer Dextromethorphan HBr Cough suppressant Doxylamine Succinate Antihistamine Multi-Symptom Relief Aches, Fever, Sore throat, Cough, Sneezing; Runny nose SOFTGELS** (**Liquid filled capsules) When using Daytime and Nighttime products, carefully read the labeling to ensure correct dosing. *This product is not manufactured or distributed by The Procter & Gamble Company.

Vicks®, DayQuil™, NyQuil™, and LiquiCaps™ are registered trademarks of the Procter and Gamble Company. TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW SIGNS OF TAMPERING. KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION Distributed by: CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895

Product Label CVS Daytime Nighttime Cold & Flu Acetaminophen 325 mg Dextromethorphan HBr 10 mg Phenylephrine HCl 5 mg Acetaminophen 325 mg Dextromethorphan HBr 15 mg Doxylamine Succinate 6.25 mg

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 HBr, Doxylamine succinate, Phenylephrine HCl — the ingredient across all brands.

Top reported reactions

Dyspnoea3
Vomiting3
Chills2
Dizziness2
Headache2
Hypersensitivity2
Nasopharyngitis2

Age at onset

Adult1
Elderly1

Reporter sex

23 reports
Male · 25%
Female · 75%

Serious outcomes

Hospitalization5
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 5 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 Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 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 CVS Pharmacy has reported a marketing end date of 2027-11-28, after which this package is expected to stop being marketed. 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 1 capsule (69842-0896-48). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
CVS Pharmacy is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 69842-0895-20 · CVS 69842-0897-24 · CVS →
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.