OTC - ACTIVE INGREDIENT SECTION
Active Ingredient/TabletAcetaminophen 110mg, Aspirin 162 mg-Salicylamide 152 mg,Pain Reviever Aid, Caffeine 32.5 mg-Pain Reliever Aid
Active Ingredient/TabletAcetaminophen 110mg, Aspirin 162 mg-Salicylamide 152 mg,Pain Reviever Aid, Caffeine 32.5 mg-Pain Reliever Aid
Purpose-Pain Reliever/Fever Reducer
Temporarily relieves pain dut to: headache, muscular aches, cold, flu. Temporarily reduces fever
Adults: Take 2 caplets every 6 hours, not to exceed 8 caplets in 24 hours
Children under 12 years, ask a doctor
Liver Warning: This product contains acetaminophen. Severe liver damage
may occur if you take:
• more than 8 tablets in 24 hours
• with other drugs containing acetaminophen (prescription or nonprescription). Ask a doctor or pharmacist before using with other drugs if you are not sure.
• 3 or more alcoholic drinks every day while using this product
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Do not use:
• with any other product containing acetaminophen this will provide more
than the recommended dose (overdose) of acetaminophen and could
cause serious health concerns.
• for more than 10 days for pain unless directed by a doctor
• for more than 3 days for fever unless directed by a doctor
• When using this product do not exceed recommended dose.
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Stop use and ask a doctor if:
• symptoms do not improve
• pain or fever persists or gets worse
• new symptoms occur
• redness or swelling is present
If pregnant or breast-feeding baby, ask a health professional
before use
KEEP OUT OF REACH OF CHILDREN. In case of overdose,
get medical help or contact a Poison Control Center right away.
Prompt medical attention is critical for adults as well as for
children even if you do not notice any signs or symptoms.
Inactive Ingredients: corn starch, microcrystalline cellulose,
povidone, croscarmellose sodium, FDC Yellow 6, magnesium stearate, and stearic acid
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 42961-042 | 42961-042-01, 42961-042-02, 42961-042-03, 42961-042-04 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| ASPIRIN | R16CO5Y76E | ACTIB |
| SALICYLAMIDE | EM8BM710ZC | ACTIB |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| FD&C YELLOW NO. 6 | H77VEI93A8 | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | 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 |
|---|---|---|---|---|---|---|
| 89edcf72-d9e0-44b1-9582-da3c50eeb556 | b632101e-2b76-4cc3-b00b-8657b23a27fe | 2022-12-30 | Warnings | b632101e-2b76-4cc3-b00b-8657b23a27fe |
Adverse event summaries are temporarily unavailable. Other product information remains available.