Indications and uses
temporarily relieves minor aches and pains due to: headache muscular aches backache minor pain of arthritis the common cold n toothache premenstrual and menstrual cramps temporarily reduces fever
Acetaminophen
- Manufacturer
- Walmart
- Effective date
- 2025-12-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- full-release
- Hydrated at
- 2026-06-01 01:27:07
Label at a glance#
ProductAcetaminophen
Active ingredientACETAMINOPHEN
Label structure17 sections
Dosage and administration
do not take more than directed (see overdose warning) adults and children 12 years and over take 2 gelcaps every 6 hours while symptoms last do not take more than 6 gelcaps 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°-25°C (68°-77°F) avoid high humidity see bottom of the label for expiration date and lot number
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each gelcap)
Acetaminophen USP, 500 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 n toothache
- premenstrual and menstrual cramps
- temporarily reduces fever
Liver warning:
This product contains acetaminophen. Severe liverdamage may occur if you take
- more than 4,000mg 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 seekmedical 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 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
- 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
- take 2 gelcaps every 6 hours while symptoms last
- do not take more than 6 gelcaps 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
Other information
- store at 20°-25°C (68°-77°F)
- avoid high humidity
- see bottom of the label for expiration date and lot number
Inactive ingredients
ammonium hydroxide, black iron oxide, colloidal silicon dioxide, croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40,
FD&C yellow #6, gelatin, hydroxypropyl cellulose, hypromellose, isopropyl alcohol, n-butyl alcohol, polyethylene glycol, povidone k-30,
pregelatinized starch, propylene glycol, red iron oxide, shellac glaze, stearic acid, titanium dioxide, yellow iron oxide
Questions or comments?
1-888-287-1915
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79903-269-10 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | 7 | |
| 79903-269-22 | Acetaminophen | 225 in 1 BOTTLE | TABLET | 225 | 7 |
Products#
Every source-derived product name is available through these pages.
- Acetaminophen
- AMMONIA
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- CROSCARMELLOSE SODIUM
- D&C RED NO. 33
- FERROSOFERRIC OXIDE
- GELATIN
- HYPROMELLOSE, UNSPECIFIED
- FERRIC OXIDE RED
- BUTYL ALCOHOL
- POLYETHYLENE GLYCOL, UNSPECIFIED
- STARCH, CORN
- PROPYLENE GLYCOL
- POVIDONE K30
- FD&C RED NO. 40
- TITANIUM DIOXIDE
- ISOPROPYL ALCOHOL
- FD&C YELLOW NO. 6
- SILICON DIOXIDE
- FERRIC OXIDE YELLOW
- SHELLAC
- STEARIC ACID
- FD&C BLUE NO. 1
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79903-269 | 79903-269-10, 79903-269-22 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Acetaminophen | ACETAMINOPHEN | Walmart | 175495fd-c561-f813-e063-6294a90aac80 | 2025-12-19 | Warnings | 79903-269-10 79903-269-22 79903-269 79903026922 79903026910 464fe735-09d4-88b8-e063-6394a90a1bc7 175495fd-c561-f813-e063-6294a90aac80 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.