Indications and uses
temporarily relieves minor aches and pains due to: -headache - muscular aches -backache -minor pain of arthritis -the common cold -toothache -premenstrual and menstrual cramps temporarily reduces fever
199 Acetaminophen 325MG Tablet
- Manufacturer
- Medline Industries, LP
- Effective date
- 2026-08-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- daily-update
- Hydrated at
- 2026-09-15 03:01:13
Label at a glance#
ProductMedline
Active ingredientACETAMINOPHEN
Label structure10 sections
Dosage and administration
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 no take more than 10 tablets in 24 hours do not use for more than 10 days unless directed by a doctor children 6-11 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 more than 5 days unless directed by a ...
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 tablet)
Acetaminophen 325 mg
Purpose
Pain reliever/fever reducer
Uses
- temporarily relieves minor aches and pains due to: -headache - muscular aches -backache -minor pain of arthritis -the common cold -toothache -premenstrual and menstrual cramps
- temporarily reduces fever
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if
- adult takes more than 4,000 mg of acetaiminophen in 24 hours
- child takes more than 5 doses in 24 hours
- 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 pharmacist
- if the user has ever had an allergic reaction to this product or any of its ingredients
Ask a doctor before use if the user
- has liver disease
- is a child with pain of arthritis
Ask a doctor or pharmacist before use if the user is
taking the blood thinning drug warfarin
Stop use and ask a doctor if
- pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
- fever gets worse or lasts more than 3 days
- new symptoms occur
- rendness 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 6-11 years |
|
| children under 6 years |
|
Other information
- store at 20-25ºC (68-77ºF)
Inactive ingredients
corscarmellose sodium*, povidone, pregelatinized starch, stearic acid
*may contain this ingredient
Questions or comments?
call 1-800-MEDLINE (633-5463) Monday - Friday, 7 a.m. to 7 p.m. CST
Manufacturing information
www.medline.com ©2026 Medline
Manufactured for: Medline Industries, LP,
Three Lakes Drive, Northfield, IL 60093 USA.
1-800-MEDLINE
**This product is not manufactured or distributed by
Johnson & Johnson Consumer Inc., distributor of
Regular Strength Tylenol® Tablets.
Package Label
Products#
Every source-derived product name is available through these pages.
- Medline
- Acetaminophen
- CROSCARMELLOSE SODIUM
- POVIDONE
- STEARIC ACID
- STARCH, CORN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53329-199 | 53329-199-30, 53329-199-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| POVIDONE | FZ989GH94E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| STARCH, CORN | O8232NY3SJ | 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.