McKesson Acetaminophen 325
- Manufacturer
- McKesson Medical-Surgical, Inc. | Unifirst Fiirst Aid Corporation
- Effective date
- 2025-09-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-06-01 01:13:19
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each tablet)
Acetaminophen 325 mg
OTC - PURPOSE SECTION
Purpose
Pain reliever/fever reducer
INDICATIONS & USAGE SECTION
Uses
temporarily relieves of minor aches and pains due to:
■ headache
■ muscular aches
■ minor arthritis pain
■ backache
■ the common cold
■ toothache
■ premenstrual and menstrual cramps
■ temporarily reduces fever
WARNINGS SECTION
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
■ more than 4,000 mg 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.
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 using and ask a doctor if
■ pain gets worse and lasts for more than 10 days
■ fever gets worse or lasts for more than 3 days
■ new symptoms occur
■ redness or swelling is present
These could be signs of a serious condition
OTC - KEEP OUT OF REACH OF CHILDREN 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.
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.
DOSAGE & ADMINISTRATION SECTION
Directions
■ do not use 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 not take more than 10 tablets 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 SAFETY INFORMATION
Other information
■ store at room temperature 59º-86ºF (15º-30ºC)
■ tamper-evident sealed packets
■ do not use any opened or torn packets
INACTIVE INGREDIENT SECTION
Inactive ingredients
corn starch, hypromellose, polyethylene glycol, povidne, pregelantinized starch, sodium starch glycolate, stearic acid, titanium dioxide
OTC - QUESTIONS SECTION
Questions or comments? Call 1-800-777-4908
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 68599-4679-9
This Package is for Households without Young Children.
McKesson
Acetaminophen
325 mg
Pain Reliever / Fever Reducer
2
Per Pack
250
Packs Per Box
MFR # 82467
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68599-4679-9 | McKesson Acetaminophen 325 | 250 in 1 BOX | TABLET, COATED | 250 | 6 | |
| 68599-4679-9 | McKesson Acetaminophen 325 | 2 in 1 PACKET | TABLET, COATED | 2 | 6 |
Products#
Every source-derived product name is available through these pages.
- McKesson Acetaminophen 325
- Acetaminophen
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL, UNSPECIFIED
- TITANIUM DIOXIDE
- POVIDONE, UNSPECIFIED
- STEARIC ACID
- STARCH, CORN
- SODIUM STARCH GLYCOLATE TYPE A POTATO
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68599-4679 | 68599-4679-9 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | 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 |
|---|---|---|---|---|---|---|
| McKesson Acetaminophen 325 | ACETAMINOPHEN | McKesson Medical-Surgical, Inc. | bc2daba5-ce8b-bbda-e053-2a95a90a6f33 | 2025-09-09 | Warnings | 68599-4679-9 68599-4679 68599467909 3e5d77e9-9141-41d7-e063-6294a90a365e bc2daba5-ce8b-bbda-e053-2a95a90a6f33 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
