Indications and uses
Uses temporarily relieves 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
479R Walg Acetaminophen Tablets 500 mg Dye Free
- Manufacturer
- WALGREENS | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
- Effective date
- 2025-12-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:22:57
Label at a glance#
ProductPain Reliever
Active ingredientACETAMINOPHEN
Label structure10 sections
Dosage and administration
Directions 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 take for more than 10 days children under 12 years ask a doctor
Contacts and useful links#
Label contents#
Full prescribing information#
Drug Facts
-
Active ingredient
Active ingredient (in each caplet)
Acetaminophen 500 mg
Purpose
Purpose
Pain reliever/fever reducer
Uses
Uses
- temporarily relieves 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 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
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.
OTC - DO NOT USE SECTION
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
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have liver disease
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin
OTC - STOP USE SECTION
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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OVERDOSAGE SECTION
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
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
Other information
- SODIUM FREE
- store between 20-25℃ (68-77℉) excursions permitted between 15-30℃ (59-86℉)
- use by expiration date on package
Inactive ingredients
Inactive ingredients hypromellose, mineral oil, povidone, pregelatinized starch, sodium starch glycolate***, stearic acid
***may contain this ingredient
OTC - QUESTIONS SECTION
Questions or comments? Call 1-877-290-4008
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0363-1137-53 | Pain Reliever | 500 in 1 BOTTLE | TABLET | 500 | 2 | |
| 0363-1137-74 | Pain Reliever | 150 in 1 BOTTLE | TABLET | 150 | 2 |
Products#
Every source-derived product name is available through these pages.
- Pain Reliever
- Acetaminophen
- STEARIC ACID
- HYPROMELLOSE, UNSPECIFIED
- STARCH, CORN
- POVIDONE
- SODIUM STARCH GLYCOLATE TYPE A CORN
- MINERAL OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0363-1137 | 0363-1137-74, 0363-1137-53 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STEARIC ACID | 4ELV7Z65AP | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| POVIDONE | FZ989GH94E | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| SODIUM STARCH GLYCOLATE TYPE A CORN | AG9B65PV6B | IACT |
| MINERAL OIL | T5L8T28FGP | 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 |
|---|---|---|---|---|---|---|
| Pain Reliever | ACETAMINOPHEN | WALGREENS | 3f9f1740-9e8b-6a2d-e063-6294a90a67cb | 2025-12-06 | Warnings | 0363-1137-53 0363-1137-74 0363-1137 00363113753 00363113774 45430c83-b1a0-6672-e063-6394a90acd3c 3f9f1740-9e8b-6a2d-e063-6294a90a67cb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.