Indications and uses
temporarily reliever 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
605 Acetaminophen 500MG Caplet
- Manufacturer
- Medline Industries, LP
- Effective date
- 2026-08-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- daily-update
- Hydrated at
- 2026-09-17 01:00:35
Label at a glance#
ProductMedline
Active ingredientACETAMINOPHEN
Label structure11 sections
Dosage and administration
do not take more than directed (see overdose warning) adults and children 12 years and over take 2 caplets every 6 hours while symptoms last do not take more than 6 caplets 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
Storage and handling
store at 20-25ºC (68-77ºF)
Contacts and useful links#
Websitewww.medline.com
www.medline.com
www.medline.comLabel contents#
Full prescribing information#
Active ingredient (in each caplet)
Acetaminophen 500 mg
Purpose
Pain reliever/fever reducer
Uses
- temporarily reliever 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
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occure 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
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.
- if you have ever had an allergic reaction to this product or any of its ingredients
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
- 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.
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).
Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Directions
- do not take more than directed (see overdose warning)
| adults and children 12 years and over |
|
| children under 12 years | ask a doctor |
Other information
- store at 20-25ºC (68-77ºF)
Inactive ingredients
carnauba wax, corn starch*, croscarmellos sodium*, hypromellose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate*, stearic acid
*may contain one or more of these ingredients
Questions or comments?
call 1-800-MEDLINE (633-5463)
Monday-Friday 7 a.m. to 7 p.m. CST
Manufacturing information
**This product is not manufactured or distributed by
Johnson & Johnson Consumer Inc., distributor of
Extra Strength Tylenol® Caplets.
www.medline.com ©2026 Medline
Manufactured for: Medline Industries, LP,
Three Lakes Drive, Northfield, IL 60093 USA
1-800-MEDLINE
Other safety information
IMPORTANT: READ ALL PRODUCT INFORMATION BEFORE USING.
KEEP THIS PACKAGE FOR IMPORTANT INFORMATION
DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING
Package label
Products#
Every source-derived product name is available through these pages.
- Medline
- Acetaminophen
- CARNAUBA WAX
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- STARCH, CORN
- STEARIC ACID
- CROSCARMELLOSE SODIUM
- SODIUM STARCH GLYCOLATE TYPE A
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53329-605 | 53329-605-30, 53329-605-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| CARNAUBA WAX | R12CBM0EIZ | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| SODIUM STARCH GLYCOLATE TYPE A | H8AV0SQX4D | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.