Home › NDC Lookup › Ingredients › Acetaminophen › 50580-0521-24
Childrens TYLENOL Acetaminophen 160 mg Tablet, Chewable, 24-count — NDC 50580-0521-24 package photo

Childrens TYLENOL Acetaminophen 160 mg Tablet, Chewable, 24-count

by Kenvue Brands LLC · 1 BOTTLE in 1 CARTON (50580-521-24) / 24 TABLET, CHEWABLE in 1 BOTTLE
NDC 50580-0521-24
🏷️ FDA NDC (as labeled) 50580-521-24 billing pads the product segment with a zero
OTC 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

⚠️
Other active recalls for Acetaminophen (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 21, 2025 — Defective Container (Kenvue Brands LLC) · FDA recall D-0121-2026
Class II · Aug 20, 2025 — Discoloration (Baxter Healthcare Corporation) · FDA recall D-0596-2025
Class II · May 22, 2025 — cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets). (Aurobindo Pharma USA Inc) · FDA recall D-0471-2025
Class I · Jul 8, 2024 — Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL) (Hikma Pharmaceuticals USA Inc.) · FDA recall D-0635-2024
Class II · May 20, 2024 — Discoloration: Brownish tablets (Contract Pharmacal Corporation) · FDA recall D-0566-2024
Class II · Nov 13, 2023 — Failed Impurities/Degradation Specifications (KINDER FARMS LLC) · FDA recall D-0143-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 50580-521-24
Product NDC 50580-521
11-digit billing NDC 50580052124
NCPDP billing unit EA — each (per item)
RxCUI 313820, 828557
UNII 362O9ITL9D
UPC 0300450519245
Application # M013
SPL Set ID b297aff8-a08b-4d37-b168-800a56564cbd
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-02-27
Route ORAL
Dosage form TABLET, CHEWABLE
Substance ACETAMINOPHEN
GPI-14 64200010000515
GCN Seq No 004493
GCN 16970
HICL code 001866
Ingredient (HICL) Acetaminophen
HIC1 code H
Therapeutic class — broad (HIC1) Nervous System (Except Autonomic)
HIC2 code H3
Therapeutic class — intermediate (HIC2) Analgesics
HIC3 code H3E
Therapeutic class — specific (HIC3) Analgesic/Antipyretics,Non-Salicylate
AHFS code 28:08.16.00
AHFS class Non-Opioid Analgesics
FDB label name CHILD TYLENOL 160 MG TAB CHEW
FDB brand name Children's Tylenol
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 50580-521-24 — 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 → 50580-0521-24. 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.

🏭 Manufacturer & labeler

LabelerKenvue Brands LLC
FDA applicationM013 (OTC MONOGRAPH DRUG)
Labeler code50580
First marketedFeb 2017
Product typeHuman Otc Drug
Portfolio564 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 CHILD TYLENOL 160 MG TAB CHEW Ingredient Acetaminophen
📖 What it is MedlinePlus · NLM

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 ↗
📗 Our plain-language guide HelloPharmacist
  • Acetaminophen is a pain reliever and fever reducer. You can use it for everyday aches like headaches, backaches, sore muscles, toothaches, minor arthritis pain, cold-related discom...
  • What is acetaminophen actually used for?
  • That's a smart thing to think about. The biggest danger with acetaminophen is taking more than the maximum daily dose allowed on your product label — especially if you're also taki...
  • How much is too much? I'm worried about taking it too often.
📖 Read our full Acetaminophen guide →
1
Nutrient depletion considerations

Acetaminophen may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Acetaminophen nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 pink
ShapeRound
ImprintTY;160;HALF;HALF
Size16 mm
ScoringScored — splits in 2
FlavorBubble Gum
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 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 3J2P07GVB6
    Cellulose acetate is a plant-derived polymer made by chemically modifying cellulose fibers. In medications, it serves as a film-coating material for tablets and capsules to protect the drug, control release, and improve appearance.
  • UNII 2S7830E561
    Crospovidone is a synthetic polymer derived from povidone. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the active ingredient can be absorbed.
  • UNII ECW0LZ41X8
    A synthetic red dye used to color tablets and capsules. It helps make medicines visually distinctive so patients can easily identify their medication.
  • UNII IY9XDZ35W2
    Dextrose is a simple sugar derived from corn or other sources. It serves as a filler and sweetener in medicines to add bulk, improve taste, and help stabilize the medication's form.
  • 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 FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • 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.

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

The official label also statesanhydrous citric acid, cellulose acetate, crospovidone, D&C red no. 7 calcium lake, dextrose, flavor, magnesium stearate, povidone, sucralose

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.
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
childrens mapap 160 mg 00904-6645-24 Major 6 tablets $0.121 — Availability likely —
Pain Relief Childrens 160 mg 46122-0424-62 Amerisource 6 tablets $0.121 — Availability likely —
Chewable Acetaminophen Childrens 160 mg 70000-0309-01 Cardinal 24 tablets $0.121 — Availability likely —
Chewable Acetaminophen Childrens 160 mg 70000-0310-01 Cardinal 24 tablets $0.121 — Availability likely —
Childrens Chewables 160 mg 70677-1127-01 Strategic 6 tablets $0.121 — Availability likely —
Childrens Pain and Fever Relief 160 mg 83324-0071-24 Chain 24 tablets $0.121 — Availability likely —
Pain and Fever Childrens 160 mg 00363-9440-08 Walgreen 6 tablets — — FDA listed —
Acetaminophen 160 mg 00363-9605-07 WALGREEN 24 tablets — — FDA listed —
Children Pain and Fever Reliver 160 mg 11673-0240-24 Target 6 tablets — — FDA listed —
Children Pain and Fever Reliever 160 mg 11673-0241-24 Target 6 tablets — — FDA listed —
pain relief childrens 160 mg 11822-4450-08 Rite 24 tablets — — FDA listed —
pain relief childrens 160 mg 11822-9440-08 Rite 24 tablets — — FDA listed —
Childrens Pain Relief 160 mg 21130-0223-76 Better 6 tablets — — FDA listed —
childrens Pain and Fever 160 mg 36800-0449-08 Topco 24 tablets — — FDA listed —
Childrens Pain and Fever 160 mg 36800-0450-08 Topco 24 tablets — — FDA listed —
Childrens Pain Reliever 160 mg 37808-0499-08 H 6 tablets — — FDA listed —
Pain Reliever Childrens 160 mg 37808-0945-08 H 6 tablets — — FDA listed —
childrens acetaminophen 160 mg 41163-0045-08 United 6 tablets — — FDA listed —
childrens acetaminophen 160 mg 41163-0494-08 United 6 tablets — — FDA listed —
Kroger Children Pain plus Fever chewables 160 mg 41226-0061-24 KROGER 6 tablets — — FDA listed —
Children Pain and Fever Reliever 160 mg 41250-0244-24 MEIJER 6 tablets — — FDA listed —
Meijer Childrens Pain and Fever Reducer 160 mg 41250-0246-24 MEIJER 6 tablets — — FDA listed —
Pain and Fever Childrens 160 mg 49035-0455-08 Wal-Mart 6 tablets — — FDA listed —
Pain and Fever Childrens 160 mg 49035-0777-08 Wal-Mart 6 tablets — — FDA listed —
Childrens TYLENOL 160 mg 50580-0517-24 Kenvue 24 tablets — — FDA listed —
Childrens TYLENOL 160 mgthis 50580-0521-24 Kenvue 24 tablets — — FDA listed —
Childrens Tylenol 160 mg 50580-0522-24 Kenvue 24 tablets — — FDA listed —
Pain and Fever Childrens 160 mg 51316-0449-08 CVS 24 tablets — — FDA listed —
Pain and Fever Chewables Childrens 160 mg 51316-0450-08 CVS 24 tablets — — FDA listed —
Childrens Chewable Acetaminophen 160 mg 53943-0449-08 Discount 24 tablets — — FDA listed —
Childrens Pain Relief 160 mg 53943-0836-76 DISCOUNT 6 tablets — — FDA listed —
Childrens Pain Relief 160 mg 53943-0837-76 DISCOUNT 6 tablets — — FDA listed —
Childrens Acetaminophen 160 mg 55301-0450-08 ARMY 24 tablets — — FDA listed —
Pain and Fever Childrens 160 mg 55910-0948-08 DOLGENCORP, 6 tablets — — FDA listed —
Childrens Pain Relief 160 mg 58602-0765-76 Aurohealth 6 tablets — — FDA listed —
Childrens Pain Relief 160 mg 58602-0766-76 Aurohealth 6 tablets — — FDA listed —
Acetaminophen 160 mg 58602-0774-82 Aurohealth 48 tablets — — FDA listed —
Non-Aspirin childrens 160 mg 63868-0186-24 CHAIN 24 tablets — — FDA listed —
childrens pain reliever 160 mg 63941-0944-08 Valu 6 tablets — — FDA listed —
childrens acetaminophen 160 mg 67091-0311-24 WinCo 6 tablets — — FDA listed —
Children Pain Relief 160 mg 69168-0440-60 Allegiant 60 tablets — — FDA listed —
Mejoralito Children CHILDREN 160 mg 69729-0160-24 OPMX 12 tablets — — FDA listed —
Resfriol-ito Children 160 mg 69729-0161-24 OPMX 12 tablets — — FDA listed —
Childrens Pain Relief 160 mg 69842-0160-24 CVS 6 tablets — — FDA listed —
Pain Relief childrens 160 mg 69842-0449-95 CVS 24 tablets — — FDA listed —
Pain Relief childrens 160 mg 69842-0450-94 CVS 24 tablets — — FDA listed —
childrens mapap 160 mg 71205-0322-24 Proficient 24 tablets — — FDA listed —
Childrens Pain and Fever 160 mg 81522-0155-24 FSA 24 tablets — — FDA listed —
Childrens Acetaminophen 160 mg 57896-0155-24 Geri-Care 24 tablets — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2017
On the market since
Feb 2017
📍
2026
Currently FDA-listed
9 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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Acetaminophen (matched by generic name) — the program that covers self-administered drugs. 5 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Acetaminophen. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$34K
Claims incl. refills
277
Beneficiaries
145
Spend / beneficiary
$234.25
Spend / claim
$122.62
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
50580-0521-24 You're viewing this 1 BOTTLE in 1 CARTON (50580-521-24) / 24 TABLET, CHEWABLE in 1 BOTTLE 2017-02-27 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 50580-521-24, 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: 50580-0521-24, written without dashes as 50580052124. 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 50580-0521-24, the first segment (50580) is the labeler code FDA assigned to Kenvue Brands LLC; the middle segment (0521) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (24) 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 Kenvue Brands LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kenvue Brands LLC 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 20 words ▾

Uses temporarily relieves minor aches and pains due to: the common cold flu headache sore throat toothache temporarily reduces fever

⏱️ Dosage and Administration 113 words ▾

Directions this product does not contain directions or complete warnings for adult use. do not give more than directed (see overdose warning ) chew or crush tablets completely before swallowing; do not swallow tablets whole find right dose on chart below. If possible, use weight to dose; otherwise, use age. repeat dose every 4 hours while symptoms last do not give more than 5 times in 24 hours Weight (lb) Age (yr) Dose (tablets) or as directed by a doctor under 24 under 2 years ask a doctor 24-35 2-3 years 1 tablet 36-47 4-5 years 1½ tablets 48-59 6-8 years 2 tablets 60-71 9-10 years 2½ tablets 72-95 11 years 3 tablets

⚠️ Warnings ~1 min read ▾

Warnings Liver warning This product contains acetaminophen. Severe liver damage may occur if your child takes more than 5 doses in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 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 your child is allergic to acetaminophen or any of the inactive ingredients in this product Ask a doctor before use if your child has liver disease Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin When using this product do not exceed recommended dose (see overdose warning ) Stop use and ask a doctor if pain gets worse or lasts more than 5 days fever gets worse or lasts more than 3 days new symptoms occur redness or swelling is present These could be signs of a serious condition.

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.

📦 Storage and Handling 26 words ▾

Other information store between 20-25°C (68-77°F). Avoid high humidity. Protect from light. do not use if foil inner seal imprinted with "TYLENOL" is broken or missing

🧪 Active Ingredient 9 words ▾

Active ingredient (in each chewable tablet) Acetaminophen 160 mg

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients anhydrous citric acid, cellulose acetate, crospovidone, D&C red no. 7 calcium lake, dextrose, flavor, magnesium stearate, povidone, sucralose

🎯 Purpose 4 words ▾

Purpose Pain reliever/fever reducer

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 50580-0517-24 · Kenvue 50580-0522-24 · Kenvue →
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.