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Pharbetol Acetaminophen 325 mg 325 mg Tablet, 100-count — NDC 73057-0353-08 package photo

Pharbetol Acetaminophen 325 mg 325 mg Tablet, 100-count

by Ulai Health LLC · 100 TABLET in 1 BOTTLE, PLASTIC (73057-353-08)
NDC 73057-0353-08
🏷️ FDA NDC (as labeled) 73057-353-08 billing pads the product segment with a zero
This package
Contains100-count Pack sizes2 compare ↓
Also comes in: 1000 tablets 73057-0353-11
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

🆔 Identity & classification

FDA NDC (as labeled) 73057-353-08
Product NDC 73057-353
11-digit billing NDC 73057035308
RxCUI 313782, 1298830
UNII 362O9ITL9D
UPC 0373057353116
Application # M013
SPL Set ID 55bb7e6c-e98c-48bd-b7bb-9848ff0273ca
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-07-08
Route ORAL
Dosage form TABLET
Substance ACETAMINOPHEN
Why two NDCs? The FDA registers this code as 73057-353-08 — 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 → 73057-0353-08. 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

LabelerUlai Health LLC
FDA applicationM013 (OTC MONOGRAPH DRUG)
Labeler code73057
First marketedJul 2019
Product typeHuman Otc Drug
Portfolio18 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

📖 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 →

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 white
ShapeRound
ImprintPH020
Size1 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 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 AG9B65PV6B
    A starch derivative made from corn that helps tablets and capsules break apart quickly when swallowed. It acts as a disintegrant, allowing the medicine to dissolve and be absorbed in your stomach and intestines.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.

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

The official label also statespovidone, pregelatinized corn starch, sodium starch glycolate, stearic acid

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: 1000 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 sense pain relief 325 mg 00113-0403-78 L. 100 tablets $0.024 — Availability likely —
Rugby Regular Strength Acetaminophen 325 mg 00536-1327-01 RUGBY 100 tablets $0.024 — Availability likely —
Acetaminophen 325 mg 00904-6773-61 Major 100 tablets $0.024 — Availability likely —
Pain Relief Regular Strength 325 mg 46122-0390-78 AmeriSource 100 tablets $0.024 — Availability likely —
Acetaminophen Regular Strength 325 mg 46122-0430-78 Amerisource 100 tablets $0.024 — Availability likely —
Acetaminophen 325 mg 49483-0340-01 TIME 100 tablets $0.024 — Availability likely —
Acetaminophen 325 mg 57237-0346-01 Rising 100 tablets $0.024 — Availability likely —
McKesson Acetaminophen 325 325 mg 68599-4679-09 McKesson 2 tablets $0.024 — Availability likely —
Pain Relief Regular Strength 325 mg 70677-1119-01 STRATEGIC 100 tablets $0.024 — Availability likely —
Acetaminophen 325 mg 82568-0001-01 AARNA 100 tablets $0.024 — Availability likely —
Pain Relief Regular Strength 325 mg 83324-0076-01 CHAIN 100 tablets $0.024 — Availability likely —
Pain Relief Regular Strength 325 mg 63868-0082-10 Chain 100 tablets $0.025 — Discontinued —
Regular Strength Acetaminophen 325 mg 70000-0092-01 CARDINAL 100 tablets $0.026 — FDA listed —
Pain Reliever 325 mg 00363-9026-10 WALGREENS 100 tablets — — FDA listed —
Henry Schein Acetaminophen 325 mg 00404-0714-13 Henry 2 tablets — — FDA listed —
Acetaminophen 325 mg 00615-8397-05 NCS 15 tablets — — FDA listed —
Acetaminophen 325 mg 00615-8398-67 NCS 60 tablets — — FDA listed —
Acetaminophen 325 mg 00615-8608-05 NCS 15 tablets — — FDA listed —
Acetaminophen 325 mg 00615-8609-67 NCS 60 tablets — — FDA listed —
Acetaminophen 325mg 325 mg 10135-0828-01 Marlex 100 tablets — — FDA listed —
Pain Relief Regular Strength 325 mg 11822-0104-01 Rite 100 tablets — — FDA listed —
Pharbetol Regular strength 325 mg 16103-0353-07 Pharbest 60 tablets — — FDA listed —
Acetaminophen 325 mg 17714-0012-01 Advance 100 tablets — — FDA listed —
Pharbetol Regular strength 325 mg 17856-0353-01 ATLANTIC 100 tablets — — FDA listed —
Pain Relief 325 mg 21130-0043-01 BETTER 100 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 30142-0052-21 KROGER 100 tablets — — FDA listed —
Aurophen Regular Strength 325 mg 30142-0184-21 KROGER 100 tablets — — FDA listed —
Pain Relief Regular Strength 325 mg 36800-0900-02 TopCo 100 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 41163-0514-02 United 100 tablets — — FDA listed —
Regular Strength Acetaminophen 325 mg 41226-0340-01 KROGER 100 tablets — — FDA listed —
pain relief 325 mg 41250-0403-78 Meijer 100 tablets — — FDA listed —
Pain Relief Regular Strength 325 mg 41250-0501-02 Meijer 100 tablets — — Discontinued —
PAIN RELIEF Regular Strength 325 mg 41520-0606-02 AMERICAN 100 tablets — — FDA listed —
Pain Relief 325 mg 42507-0501-02 HYVEE 100 tablets — — FDA listed —
Medique APAP 325 mg 47682-0057-13 Unifirst 2 tablets — — FDA listed —
Medi-First Non-Aspirin 325 mg 47682-0058-13 Unifirst 2 tablets — — FDA listed —
Medi-First Plus Non-Aspirin 325 mg 47682-0059-33 Unifirst 2 tablets — — FDA listed —
Dover Aminofen 325 mg 47682-0060-13 Unifirst 2 tablets — — FDA listed —
Medique APAP 325 mg 47682-0145-13 Unifirst 2 tablets — — FDA listed —
Dover Aminophen 325 mg 47682-0303-13 Unifirst 2 tablets — — FDA listed —
Medique at Home APAP 325 mg 47682-0434-33 Unifirst 2 tablets — — FDA listed —
Medi-First Non-Aspirin 325 mg 47682-0803-13 Unifirst 2 tablets — — FDA listed —
MEDI FIRST PLUS Non-Aspirin 325 mg 47682-0903-33 Unifirst 2 tablets — — FDA listed —
Ringl 325 mg 49873-0082-01 Sato 30 tablets — — FDA listed —
Rugby Regular Strength Acetaminophen 325 mg 50090-5971-06 A-S 50 tablets — — FDA listed —
Cetafen 325 mg 50332-0148-01 HART 1000 tablets — — FDA listed —
TYLENOL Regular Strength 325 mg 50580-0458-10 Kenvue 1000 tablets — — Discontinued —
TYLENOL Regular Strength 325 mg 50580-0475-10 Kenvue 1000 tablets — — FDA listed —
TYLENOL Regular Strength 325 mg 50580-0495-01 Kenvue 100 tablets — — FDA listed —
TYLENOL Regular Strength 325 mg 50580-0496-60 Kenvue 100 tablets — — FDA listed —
MEDIQUE APAP acetaminophen 325 mg 51662-1273-02 HF 2 tablets — — FDA listed —
acetaminophen 325 mg 51662-1665-02 HF 2 tablets — — FDA listed —
CareALL Acetaminophen 325 mg 51824-0061-02 New 2400 tablets — — FDA listed —
CareALL Acetaminophen 325 mg 51824-0085-01 New 100 tablets — — FDA listed —
Duralgina 325 mg 53145-0013-71 Menper 30 tablets — — FDA listed —
Clear Choice Regular Strength Pain Reliever 325 mg 53185-0005-00 Athlete's 100 tablets — — FDA listed —
Medline 325 mg 53329-0194-30 Medline 100 tablets — — FDA listed —
Pain Relief 325 mg 53942-0101-02 Demoulas 100 tablets — — FDA listed —
Pain Relief 325 mg 53943-0201-02 DISCOUNT 100 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 54257-0720-02 Magno-Humphries, 100 tablets — — FDA listed —
Acetaminophen 325 mg 54738-0548-01 Richmond 100 tablets — — FDA listed —
Acetaminophen 325 mg 55154-7899-00 Cardinal 10 tablets — — FDA listed —
Acetaminophen Regular strength 325 mg 55289-0563-01 PD-Rx 100 tablets — — FDA listed —
dg health pain relief 325 mg 55910-0697-78 Dolgencorp, 100 tablets — — FDA listed —
Pain Relief 325 mg 57344-0301-06 AAA 500 tablets — — FDA listed —
Regular Strength Pain Relief 325 mg 57896-0102-01 Geri-Care 100 tablets — — FDA listed —
Acetaminophen 325 mg 58228-0061-01 Prostat 20000 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 58602-0748-40 Aurohealth 500 tablets — — FDA listed —
Aurophen Regular Strength 325 mg 58602-0754-07 Aurohealth 24 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 58602-0775-21 Aurohealth 100 tablets — — FDA listed —
Travel Savvy Non-Aspirin 325 mg 59961-0151-15 Bellegrove 2 tablets — — FDA listed —
Direct Safety Aspirin Free 325 mg 61245-0145-13 Conney 2 tablets — — FDA listed —
Regular Strength Pain Reliever 325 mg 62936-0102-01 INGLES 100 tablets — — FDA listed —
Regular Strength Pain Relief 325 mg 63941-0456-02 VALU 100 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 67091-0132-10 WinCo 100 tablets — — FDA listed —
Acetaminophen 325 mg 68071-3454-03 NuCare 30 tablets — — FDA listed —
Regular Strength Pain Relief 325 mg 68071-3565-00 NuCare 100 tablets — — FDA listed —
good sense pain relief 325 mg 68071-3883-02 NuCare 20 tablets — — FDA listed —
good sense pain relief 325 mg 68071-3917-06 NuCare 6 tablets — — FDA listed —
Regular Strength Pain Relief 325 mg 68071-4656-05 NuCare 50 tablets — — FDA listed —
DRX CHOICE Regular Strength 325 mg 68163-0065-60 Raritan 60 tablets — — FDA listed —
good sense pain relief 325 mg 68788-8821-01 Preferred 100 tablets — — FDA listed —
Pain Relief Regular Strength 325 mg 68998-0301-01 MARC 100 tablets — — FDA listed —
Acetaminophen 325mg RS 325 mg 69168-0010-30 Allegiant 30 tablets — — FDA listed —
Acetaminophen 325 Mg 69618-0010-01 Reliable 100 tablets — — FDA listed —
Acetaminophen 325 mg 69822-0692-10 Southern 325 tablets — — FDA listed —
Acetaminophen Regular Strength 325 mg 69842-0876-51 CVS 365 tablets — — FDA listed —
Acetaminophen 325 mg 69842-0968-01 CVS 100 tablets — — FDA listed —
Regular Strength Pain Reliever 325 mg 70677-1243-01 Strategic 120 tablets — — FDA listed —
MEDI-FIRST Non-Aspirin 325 mg 71205-0306-04 Proficient 4 tablets — — FDA listed —
Acetaminophen 325 Mg 71205-0456-00 Proficient 100 tablets — — FDA listed —
good sense pain relief 325 mg 71335-2574-01 Bryant 100 tablets — — FDA listed —
Acetaminophen 325 mg 71335-2747-00 Bryant 24 tablets — — FDA listed —
Acetaminophen 325 mg 71335-3130-00 Bryant 24 tablets — — FDA listed —
Acetaminophen 325 mg 71399-1025-01 Akron 100 tablets — — FDA listed —
Acetaminophen 325 mg 71610-0238-65 Aphena 100 tablets — — FDA listed —
Acetaminophen 325 mg 71679-0305-00 Health 47000 tablets — — FDA listed —
Acetaminophen 325 mg 72036-0100-02 HARRIS 100 tablets — — FDA listed —
Regular Strength Pain Relief 325 mg 72162-2252-01 Bryant 100 tablets — — FDA listed —
basic care acetaminophen 325 mg 72288-0403-78 Amazon.com 100 tablets — — FDA listed —
Amazon Basic Care Acetaminophen 325 mg 72288-0405-10 Amazon.com 100 tablets — — FDA listed —
Acetaminophen 325 mg 72789-0267-20 PD-Rx 20 tablets — — FDA listed —
Pharbetol 325 mgthis 73057-0353-08 Ulai 100 tablets — — FDA listed —
Aphen 325 mg 76420-0372-15 Asclemed 150 tablets — — FDA listed —
Pain Reliever 325 mg 79903-0130-99 WAL-MART 100 tablets — — FDA listed —
equate pain reliever 325 mg 79903-0299-10 WALMART 100 tablets — — FDA listed —
Dr Simi Pain Relief 325 mg 85786-0103-90 Farmacias 100 tablets — — FDA listed —
Acetaminophen 325 mg 85828-0102-02 Grocery 100 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

🏛️
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.

🔬 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 Pharbetol (this brand).

Top reported reactions

Fatigue20,911
Pain18,475
Nausea18,193
Headache17,145
Toxicity To Various Agents15,844
Dyspnoea15,032
Pyrexia14,589

Reporter sex

253,903 reports
Male · 38%
Female · 62%
Unknown · 0%

Serious outcomes

Hospitalization114,395
Death50,001
Life-threatening21,915
Disabling12,035
Reports over time (by year) — tap or hover for the count & year
2024 2025 2026 28,623 13,418
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73057-0353-08 You're viewing this 100 TABLET in 1 BOTTLE, PLASTIC (73057-353-08) 2019-07-08 Active
73057-0353-11 1000 TABLET in 1 BOTTLE, PLASTIC (73057-353-11) 2019-07-08 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 73057-0353-08?
NDC 73057-0353-08 is a 100-count package — 100 tablet in 1 bottle, plastic.
What is the difference between NDC 73057-0353-08 and NDC 73057-0353-11?
Both are Pharbetol Acetaminophen 325 mg 325 mg Tablet — the drug itself is identical. NDC 73057-0353-08 is the 100-count package, while NDC 73057-0353-11 is the 1000 tablets package.
What NDC number is used to bill for this package of Pharbetol Acetaminophen 325 mg 325 mg Tablet?
Bill NDC 73057-0353-08 — the 11-digit billing format is 73057035308. 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

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 73057-353-08, 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: 73057-0353-08, written without dashes as 73057035308. 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 73057-0353-08, the first segment (73057) is the labeler code FDA assigned to Ulai Health LLC; the middle segment (0353) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) 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 Ulai Health LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1000 tablets (73057-0353-11). 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?
Ulai Health 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 28 words ▾

Uses temporarily relieves minor aches and pains due to: the common cold headache backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever

⏱️ Dosage and Administration 103 words ▾

Directions do not take more than directed (see overdose warning) adults and children 12 years and over take 2 tablets every 4 to 6 hours while symptoms last do not take more than 10 tablets in 24 hours, unless directed by a doctor do not use for more than 10 days unless directed by a doctor children 6 to under 12 years take 1 tablet every 4 to 6 hours while symptoms last do not take more than 5 tablets in 24 hours do not use for more than 5 days unless directed by a doctor children under 6 years ask a doctor

⚠️ Warnings ~1 min read ▾

Warnings Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. 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, which is the maximum daily amount 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. 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 a pharmacist. if you are allergic to acetaminophen or any of the inactive ingredients in this product Ask a doctor before use if you have liver disease.

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin. Stop use and ask a doctor if pain gets worse or lasts more than 10 days in adults pain gets worse or lasts more than 5 days in children under 12 years fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur 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).

📦 Storage and Handling 10 words ▾

Other information store at 20-25 0 C (68-77 0 F)

🧪 Active Ingredient 8 words ▾

Active ingredient (in each tablet) Acetaminophen 325 mg

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients povidone, pregelatinized corn starch, sodium starch glycolate, stearic acid

🎯 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 ↗
← 73057-0352-03 · Ulai 73057-0356-09 · Ulai →
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.