Storage and handling
Other information store at room temperature
Other information store at room temperature
Drug Facts
Active ingredient (in each tablet)
Acetaminophen 325 mg
Purposes
Pain reliever/fever reducer
Uses
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if
Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
Ask a doctor before use if the user has liver disease.
Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin.
Stop use and ask a doctor if
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
| adults and children 12 years and over |
|
| children 6 years to under 12 years |
|
| children under 6 years | ask a doctor |
Other information
Inactive ingredients Povidone, pregelatinized starch, sodium starch glycolate, stearic acid
Questions or Comments?
call (800) 795-9775
Do not use if carton is open, or if imprinted safety seal under cap is broken or missing
NDC 70000-0152-1
Leader™
Regular Strength
Acetaminophen
Tablets, 325 mg | Pain Reliever / Fever Reducer
For Relief of:
Headache, Fever, Aches and Pains
Aspirin Free
24 TABLETS
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0152-1 | EA - Each | 70000-0152 | 4a3604d8-4345-42c4-8889-e588e486f066 | 1 | 2017-12-14 |
| 70000-0152-2 | EA - Each | 70000-0152 | ab2ee89f-8316-41a5-b9f7-85e909673119 | 1 | 2017-12-14 |
| 70000-0152-3 | EA - Each | 70000-0152 | dd0b2d5d-7ef7-499e-a677-550116f9f341 | 1 | 2017-12-14 |
| 70000-0152-4 | EA - Each | 70000-0152 | 5ae29dcd-ad10-475a-b76b-67b5331b9b2f | 1 | 2017-12-14 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70000-0152 | 70000-0152-1, 70000-0152-3, 70000-0152-2, 70000-0152-4 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STARCH, PREGELATINIZED CORN | O8232NY3SJ | IACT |
| POVIDONE | FZ989GH94E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
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 |
|---|---|---|---|---|---|---|
| 74834e1b-0d7c-0542-e053-2991aa0aa1ef | 42629fcd-d79a-0763-e054-00144ff8d46c | 2018-08-28 | Warnings | 74834e1b-0d7c-0542-e053-2991aa0aa1ef 42629fcd-d79a-0763-e054-00144ff8d46c |
Adverse event summaries are temporarily unavailable. Other product information remains available.