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Drug Facts

Manufacturer
Wildman Business Group | Future Pak, Ltd. | LNK International, Inc.
Effective date
2026-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-17 21:45:49

Label at a glance#

ProductAcetaminophen
Active ingredientAcetaminophen
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains associated with: Headache minor arthritis pain toothache menstrual cramps muscular aches common cold

Dosage and administration

Do not use more than directed take 2 tablets every 6 hours while symptoms persist or as directed by a doctor. do not take more than 6 tablets in 24 hours, unless directed by a doctor do not use for more than 10 days unless directed by a doctor Children under 12 years:  Ask a doctor

Label contents#

Full prescribing information#

Active Ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen

Purpose

OTC - PURPOSE SECTION

Pain reliever / fever reducer

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains associated with:

  • Headache
  • minor arthritis pain
  • toothache
  • menstrual cramps
  • muscular aches
  • common cold

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Liver warning: This product contains 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 this product

SPL UNCLASSIFIED SECTION

Allergy alert: Acetaminophen may cause 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:

OTC - DO NOT USE SECTION

  • 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 allergic to acetaminophen or any of the inactive ingredients in this product

Ask a doctor before use if you have:

OTC - ASK DOCTOR SECTION

  • Liver disease

Ask a doctor or pharmacist before us if you are:

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking the blood thinning drug warfarin

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • pain gets worse or lasts more than 10 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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Do not use more than directed

Adults and children 12 years and over

SPL UNCLASSIFIED SECTION

  • take 2 tablets every 6 hours while symptoms persist or as directed by a doctor.
  • do not take more than 6 tablets in 24 hours, unless directed by a doctor
  • do not use for more than 10 days unless directed by a doctor

SPL UNCLASSIFIED SECTION

Children under 12 years: Ask a doctor

Other information:

OTHER SAFETY INFORMATION

  • store at room temperature 59º-86ºF (15º-30ºC)
  • tamper-evident sealed packets
  • do not use any opened or torn packets

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Corn starch, unspecified povidone, sodium starch glycolate, stearic acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

Compare to Tylenol

2522

ProvisionPlus

Maximum Strength

Non-Aspirin

Relief for Minor Aches and Pains

Temporary Relief of:

Headaches

Toothaches

Minor Pains

Fever

250 tablets

2 Per Packet

Principal Display Panel – 250 Tablet Box Label
Principal Display Panel – 250 Tablet Box Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84269-252284269-2522-2, 84269-2522-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Acetaminophen362O9ITL9DACTIB
STARCH, CORNO8232NY3SJIACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
SODIUM STARCH GLYCOLATE TYPE A POTATO5856J3G2A2IACT
STEARIC ACID4ELV7Z65APIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-05-20full-release2026-06-01 00:12:51

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenACETAMINOPHENWildman Business Group943c8f49-e65e-40bc-b364-3274df4d21a22026-07-09WarningsExact identifier
ndc (package): 84269-2522-1
ndc (package): 84269-2522-2
ndc (product): 84269-2522
ndc11 (package): 84269252201
ndc11 (package): 84269252202
spl id: 35f6a135-2698-41bb-956f-0f76402dae34
spl set id: 943c8f49-e65e-40bc-b364-3274df4d21a2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.