Indications and uses
For the temporary relief of minor aches and pains associated with headache toothache minor arthritis pain muscular aches the common cold menstrual cramps For the reduction of fever.
Pain Reliever
- Manufacturer
- L.N.K. International, Inc. | LNK International, Inc.
- Effective date
- 2023-12-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:17:35
Label at a glance#
ProductPain Reliever
Active ingredientACETAMINOPHEN
Label structure9 sections
Dosage and administration
do not use more than directed Adults and children 12 years and over: Take 2 tablets every 4 to 6 hours as needed. Do not take more than 8 tablets in 24 hours. Children under 12 years: Do not give this adult strength product to children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.
Storage and handling
store at room temperature 59 ̊-86 ̊F (15 ̊-30 ̊C) tamper-evident sealed packets do not use any opened or torn packets
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each tablet)
Acetaminophen 500 mg
Purpose
Pain reliever/fever reducer
Uses
For the temporary relief of minor aches and pains associated with
- headache
- toothache
- minor arthritis pain
- muscular aches
- the common cold
- menstrual cramps
For the reduction of fever.
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 8 tablets in 24 hours, which is the maximum daily amount
- with other drugs containing acetaminophen
- 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 pharmacist.
- for more than 10 days for pain unless directed by a doctor
- for more than 3 days for fever unless directed by a doctor
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
- symptoms do not improve
- new symptoms occur
- pain or fever persists or gets worse
- redness or swelling is present
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
In case of accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Directions
- do not use more than directed
Adults and children 12 years and over:
| Take 2 tablets every 4 to 6 |
Children under 12 years: | Do not give this adult strength product to children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage. |
Other information
- store at room temperature 59 ̊-86 ̊F (15 ̊-30 ̊C)
- tamper-evident sealed packets
- do not use any opened or torn packets
Inactive ingredients
corn starch, hypromellose, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone*, pregelatinized starch*, sodium starch glycolate*, stearic acid, titanium dioxide*
*may contain
Questions or comments?
1-800-426-9391
Principal display panel
QUALITY
PLUS
NDC 50844-270-24
†Compare to active ingredient in Extra Strength Tylenol®
EXTRA STRENGTH
PAIN RELIEVER
Acetaminophen 500 mg
PAIN RELIEVER/FEVER REDUCER
CONTAINS NO ASPIRIN
60 Packets
of 2 Tablets each
500 mg each
ACTUAL SIZE
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED
OR IF PACKET IS TORN, BROKEN OR SHOWS ANY SIGNS
OF TAMPERING
†This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Extra Strength Tylenol®.
50844 ORG
Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive Hauppauge, NY 11788 USA
Products#
Every source-derived product name is available through these pages.
- Pain Reliever
- Acetaminophen
- STARCH, CORN
- HYPROMELLOSE, UNSPECIFIED
- MALTODEXTRIN
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STEARIC ACID
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50844-270 | 50844-270-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| STARCH, CORN | O8232NY3SJ | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0dcdc9ff-4f19-4162-b6ac-528c81501157 | 5aa8d99b-7a38-4f01-a95f-baf0f57296ed | 2024-06-17 | Warnings | 5aa8d99b-7a38-4f01-a95f-baf0f57296ed |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.