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up and up ibuprofen pm diphenhydramine citrate 38 mg; 200 mg Tablet, Film Coated, 20-count — NDC 11673-0050-60 package photo

up and up ibuprofen pm diphenhydramine citrate 38 mg; 200 mg Tablet, Film Coated, 20-count

by Target Corporation · 1 BOTTLE in 1 CARTON (11673-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE
NDC 11673-0050-60
🏷️ FDA NDC (as labeled) 11673-050-60 billing pads the product segment with a zero
This package
Contains20-count Pack sizes4 compare ↓
Also comes in: 40 tablets 11673-0050-58 120 tablets 11673-0050-76 200 tablets 11673-0050-82
OTC Generic 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 11673-050-60
Product NDC 11673-050
11-digit billing NDC 11673005060
RxCUI 895664
UNII 4OD433S209, WK2XYI10QM
Application # ANDA079113
SPL Set ID 0c764683-f3c9-4382-96be-d34b7a582aee
Established class (EPC) Nonsteroidal Anti-inflammatory Drug
Mechanism of action Cyclooxygenase Inhibitors
Chemical class Anti-Inflammatory Agents, Non-Steroidal
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2009-07-10
Route ORAL
Dosage form TABLET, FILM COATED
Substance DIPHENHYDRAMINE CITRATE; IBUPROFEN
GPI-14 60309902400320
GPI class TGT Ibuprofen PM
GCN Seq No 062493
GCN 98268
HICL code 034634
Ingredient (HICL) Ibuprofen/Diphenhydramine Cit
HIC1 code S
Therapeutic class — broad (HIC1) Locomotor System
HIC2 code S2
Therapeutic class — intermediate (HIC2) Drugs Acting Principally On Joints
HIC3 code S2S
Therapeutic class — specific (HIC3) Analgesic,Nsaid-1St Gen.antihistamine,Sedative Cmb
AHFS code 04:04.04.00
AHFS class Ethanolamine Derivatives
FDB label name IBUPROFEN PM CAPLET
FDB brand name Ibuprofen Pm
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 11673-050-60 — 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 → 11673-0050-60. 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 Histamine-1 Receptor Antagonist class.

Pharmacologic class Histamine-1 Receptor Antagonist
Drug family (ATC) Propionic acid derivatives, Antihistamines for topical use, Aminoalkyl ethers
How it works Histamine H1 Receptor Antagonists
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

LabelerTarget Corporation
Application holderPERRIGO R AND D CO
FDA applicationANDA079113 (ANDA)
Labeler code11673
First marketedJul 2009
Product typeHuman Otc Drug
Portfolio408 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 IBUPROFEN PM CAPLET Ingredient Ibuprofen/Diphenhydramine Cit
📖 What it is MedlinePlus · NLM

Diphenhydramine is used to treat allergy and cold symptoms: sneezing runny nose red, itchy, watery eyes itching of the nose or throat Diphenhydramine is also used to treat insomnia (difficulty falling asleep or staying asleep) in adults, but should not be used to make a child sleepy. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms. Diphenhydramine is also available in combination with other medications. This monograph only includes information about the use of diphenh...

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • No — this product is specifically for nights when you have both minor pain AND trouble sleeping at the same time. It's not meant to be used as a plain sleep aid. If you're struggli...
  • What exactly is this medicine for — can I just take it to help me sleep?
  • Take 2 capsules or caplets at bedtime — whichever form your product comes in. Don't take more than that in 24 hours. If it bothers your stomach, go ahead and take it with food or a...
  • How do I take it, and is it okay to take with food?
📖 Read our full Diphenhydramine / Ibuprofen guide →

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 Blue
ShapeOval
ImprintL050
Size15 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.

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

  • UNII M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • UNII L06K8R7DQK
    A synthetic blue dye approved by the FDA for use in medications and foods. It serves as a colorant to make pills and liquids visually distinct and easier to identify.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII R8WTH25YS2
    Glyceryl dibehenate is a wax-like substance made from behenate fatty acids and glycerol. It functions as a binder and release-control agent in tablets and capsules, helping hold ingredients together and regulate how quickly the medicine dissolves and releases in your body.
  • UNII 9XZ8H6N6OH
    A plant-based cellulose derivative used as a binder to hold tablet ingredients together, a thickener in liquids, and a coating agent to control how fast the medicine dissolves.
  • UNII EWQ57Q8I5X
    Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • 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 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

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

The official label also statescolloidal silicon dioxide, croscarmellose sodium, FD&C blue no. 2 aluminum lake, glyceryl behenate, hydroxypropyl cellulose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, talc, titanium dioxide

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 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: 40 tablets 120 tablets 200 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
good neighbor pharmacy ibuprofen pm 38 mg/1; 200 mg 46122-0708-41 Amerisource 80 tablets $0.122 — Discontinued —
Leader Ibuprofen PM 38 mg/1; 200 mg 70000-0157-01 Cardinal 40 tablets $0.125 — Availability likely —
good sense ibuprofen pm 38 mg/1; 200 mg 00113-0050-58 L. 40 tablets $0.131 — Availability likely —
foster and thrive ibuprofen pm 38 mg/1; 200 mg 70677-1131-01 Strategic 40 tablets $0.131 — Availability likely —
Ibuprofen PM 38 mg/1; 200 mg 00363-0050-27 Walgreen 80 tablets — — FDA listed —
Advil Pm 38 mg/1; 200 mg 00573-0164-04 Haleon 4 tablets — — FDA listed —
up and up ibuprofen pm 38 mg/1; 200 mgthis 11673-0050-60 Target 20 tablets — — FDA listed —
ibuprofen pm 38 mg/1; 200 mg 11822-0050-01 Rite 80 tablets — — Discontinued —
Ibuprofen PM 200 mg/1; 38 mg 21130-0056-40 Safeway, 40 tablets — — FDA listed —
Ibuprofen and Diphenhydramine Citrate 200 mg/1; 38 mg 21130-0228-12 Better 40 tablets — — FDA listed —
Signature Care Ibuprofen PM 38 mg/1; 200 mg 21130-0283-27 Safeway 80 tablets — — Discontinued —
Ibuprofen Pm 38 mg/1; 200 mg 21130-0623-76 Safeway 120 tablets — — FDA listed —
ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated 38 mg/1; 200 mg 29485-6533-04 Lil 2 tablets — — FDA listed —
ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated 38 mg/1; 200 mg 29485-7008-03 Lil 2 tablets — — FDA listed —
ibuprofen pm 38 mg/1; 200 mg 30142-0050-27 Kroger 80 tablets — — FDA listed —
Ibuprofen PM 200 mg/1; 38 mg 30142-0278-80 KROGER 80 tablets — — FDA listed —
Topcare Ibuprofen PM 38 mg/1; 200 mg 36800-0050-27 Topco 80 tablets — — FDA listed —
ibuprofen pm 38 mg/1; 200 mg 37808-0703-60 H 20 tablets — — FDA listed —
equaline ibuprofen pm 38 mg/1; 200 mg 41163-0050-27 United 80 tablets — — FDA listed —
Ibuprofen PM 38 mg/1; 200 mg 41250-0050-27 Meijer 80 tablets — — Discontinued —
Care One Ibuprofen PM 38 mg/1; 200 mg 41520-0050-27 American 80 tablets — — FDA listed —
ibuprofen pm 38 mg/1; 200 mg 42507-0050-27 HyVee 80 tablets — — FDA listed —
equate ibuprofen pm 38 mg/1; 200 mg 49035-0699-27 Wal-Mart 80 tablets — — FDA listed —
Motrin PM 200 mg/1; 38 mg 50580-0563-20 Kenvue 20 tablets — — FDA listed —
Ibuprofen and Diphenhydramine Citrate 200 mg/1; 38 mg 55111-0565-05 Dr. 500 tablets — — FDA listed —
Exchange Select Ibuprofen PM 38 mg/1; 200 mg 55301-0050-60 Army 20 tablets — — FDA listed —
Ibuprofen PM 200 mg/1; 38 mg 55319-0197-20 Family 20 tablets — — FDA listed —
dg health Ibuprofen pm 38 mg/1; 200 mg 55910-0050-27 Dolgencorp 80 tablets — — FDA listed —
Ibuprofen and Diphenhydramine Citrate 200 mg/1; 38 mg 58602-0867-09 Aurohealth 30 tablets — — FDA listed —
ibuprofen pm 38 mg/1; 200 mg 59779-0050-27 CVS 80 tablets — — FDA listed —
Ibuprofen 200 mg and Diphenhydramine Citrate 38 mg 200 mg/1; 38 mg 63548-0197-02 PLD 20 tablets — — FDA listed —
Advil PM, TRAVEL BASIX 200 mg/1; 38 mg 66715-6433-02 Lil' 2 tablets — — FDA listed —
Advil PM, CVP HEALTH 200 mg/1; 38 mg 66715-6533-02 Lil' 2 tablets — — FDA listed —
Advil PM 200 mg/1; 38 mg 66715-9633-03 Lil' 2 tablets — — FDA listed —
Advil PM 200 mg/1; 38 mg 66715-9733-02 Lil' 2 tablets — — FDA listed —
Advil PM 38 mg/1; 200 mg 67751-0147-01 Navajo 2 tablets — — FDA listed —
Ibuprofen PM 200 mg/1; 38 mg 69607-1970-01 WR 120 tablets — — FDA listed —
basic care ibuprofen pm 38 mg/1; 200 mg 72288-0050-60 Amazon.com 20 tablets — — FDA listed —
Amazon Basic Care Ibuprofen Pm 200 mg/1; 38 mg 72288-0061-77 Amazon.com 120 tablets — — FDA listed —
Ibuprofen PM 200 mg/1; 38 mg 79903-0186-20 WALMART 20 tablets — — FDA listed —
Advil Pm 38 mg/1; 200 mg 85237-1784-01 Select 2 tablets — — FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
2009
On the market since
Jul 2009
📍
2026
Currently FDA-listed
17 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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 NDCDescription Marketing startStatus
11673-0050-58 1 BOTTLE in 1 CARTON (11673-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE 2009-07-24 Active
11673-0050-76 1 BOTTLE in 1 CARTON (11673-050-76) / 120 TABLET, FILM COATED in 1 BOTTLE 2017-02-07 Discontinued by firm
11673-0050-82 200 TABLET, FILM COATED in 1 BOTTLE (11673-050-82) 2022-01-27 Active
11673-0050-60 You're viewing this 1 BOTTLE in 1 CARTON (11673-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE 2026-03-10 Active

Pack size FAQ

What quantity is in NDC 11673-0050-60?
NDC 11673-0050-60 is a 20-count package — 1 bottle in 1 carton / 20 tablet, film coated in 1 bottle.
What is the difference between NDC 11673-0050-60 and NDC 11673-0050-58?
Both are up and up ibuprofen pm diphenhydramine citrate 38 mg; 200 mg Tablet, Film Coated — the drug itself is identical. NDC 11673-0050-60 is the 20-count package, while NDC 11673-0050-58 is the 40 tablets package.
What NDC number is used to bill for this package of up and up ibuprofen pm diphenhydramine citrate 38 mg; 200 mg Tablet, Film Coated?
Bill NDC 11673-0050-60 — the 11-digit billing format is 11673005060. 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 ✓ 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 11673-050-60, 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: 11673-0050-60, written without dashes as 11673005060. 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 11673-0050-60, the first segment (11673) is the labeler code FDA assigned to Target Corporation; the middle segment (0050) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (60) 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 Target 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 3 other package presentations of this same product, including 40 tablets (11673-0050-58), 120 tablets (11673-0050-76), 200 tablets (11673-0050-82). 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?
Target 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 22 words ▾

Uses • for relief of occasional sleeplessness when associated with minor aches and pains • helps you fall asleep and stay asleep

⏱️ Dosage and Administration 32 words ▾

Directions • do not take more than directed • adults and children 12 years and over: take 2 caplets at bedtime • do not take more than 2 caplets in 24 hours

⚠️ Warnings ~3 min read ▾

Warnings Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives • facial swelling • asthma (wheezing) • shock • skin reddening • rash • blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding.

The chance is higher if you • are age 60 or older • have had stomach ulcers or bleeding problems • take a blood thinning (anticoagulant) or steroid drug • take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others] • have 3 or more alcoholic drinks every day while using this product • take more or for a longer time than directed Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use • if you have ever had an allergic reaction to any other pain reliever/fever reducer • unless you have time for a full night’s sleep • in children under 12 years of age • right before or after heart surgery • with any other product containing diphenhydramine, even one used on skin • if you have sleeplessness without pain Ask a doctor before use if • stomach bleeding warning applies to you • you have problems or serious side effects from taking pain relievers or fever reducers • you have a history of stomach problems, such as heartburn • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke • you are taking a diuretic • you have a breathing problem such as emphysema or chronic bronchitis • you have glaucoma • you have trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are • taking sedatives or tranquilizers, or any other sleep-aid • under a doctor’s care for any continuing medical illness • taking any other antihistamines • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin • taking any other drug When using this product • drowsiness will occur • avoid alcoholic drinks • do not drive a motor vehicle or operate machinery • take with food or milk if stomach upset occurs Stop use and ask a doctor if • you experience any of the following signs of stomach bleeding: • feel faint • vomit blood • have bloody or black stools • have stomach pain that does not get better • you have symptoms of heart problems or stroke: • chest pain • trouble breathing • weakness in one part or side of body • slurred speech • leg swelling • pain gets worse or lasts more than 10 days • sleeplessness persists continuously for more than 2 weeks.

Insomnia may be a symptom of a serious underlying medical illness. • redness or swelling is present in the painful area • any new symptoms appear If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery. Keep out of the reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

📦 Storage and Handling 25 words ▾

Other information • read all warnings and directions before use. Keep carton. • store at 20-25°C (68 -77°F) • avoid excessive heat above 40°C (104°F)

🧪 Active Ingredient 16 words ▾

Active ingredients (in each caplet) Diphenhydramine citrate 38 mg Ibuprofen 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug

🧪 Inactive Ingredients 35 words ▾

Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, FD&C blue no. 2 aluminum lake, glyceryl behenate, hydroxypropyl cellulose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, talc, titanium dioxide

🎯 Purpose 5 words ▾

Purposes Nighttime sleep-aid Pain reliever

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 11673-0049-06 · TARGET 11673-0051-90 · Target →
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.