Indications and uses
temporarily relieves minor aches and pains due to: the common cold headache minor pain of arthritis backache muscular aches toothache premenstrual and menstrual cramps temporarily reduces fever
Perrigo Pain Relief Tablets Drug Facts
- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Effective date
- 2025-08-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:09:55
Label at a glance#
Productgood sense pain relief
Active ingredientACETAMINOPHEN
Label structure8 sections
Dosage and administration
do not take 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 do not use for more than 10 days unless directed by a doctor children 6-11 years take 1 tablet every 4 to 6 hours while symptoms last do not take more than 5 tablets in 24 hours do not use for more than 5 days unless directed ...
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each tablet)
Acetaminophen 325 mg
Purpose
Pain reliever/fever reducer
Uses
- temporarily relieves minor aches and pains due to:
- the common cold
- headache
- minor pain of arthritis
- backache
- muscular aches
- toothache
- premenstrual and menstrual cramps
- temporarily reduces fever
Warnings
Liver warning:This product contains acetaminophen. Severe liver damage may occur if
- adult takes more than 4,000 mg of acetaminophen in 24 hours
- child takes more than 5 doses in 24 hours
- taken with other drugs containing acetaminophen
- adult has 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.
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 the user has ever had an allergic reaction to this product or any of its ingredients
Ask a doctor before use if the user
- has liver disease
- is a child with pain of arthritis
Ask a doctor or pharmacist before use if the user is
taking the blood thinning drug warfarin
Stop use and ask a doctor if
- new symptoms occur
- pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
- fever gets worse or lasts more than 3 days
- 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 |
| |
children 6-11 years |
| |
children under 6 years | ask a doctor |
Inactive ingredients
croscarmellose sodium*, povidone, pregelatinized starch, stearic acid *may contain this ingredient
Questions or comments?
1-800-719-9260
Principal Display Panel
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-3883-2 | good sense pain relief | 1 in 1 CARTON | TABLET | 1 | 1 | |
| 68071-3883-2 | good sense pain relief | 20 in 1 BOTTLE | TABLET | 20 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0113-0403-78 | EA - Each | 0113-0403 | 6e8d8f22-2a1f-4f1b-bfb4-b913ba35bc9c | 1 | 2019-09-05 |
Products#
Every source-derived product name is available through these pages.
- good sense pain relief
- Acetaminophen
- CROSCARMELLOSE SODIUM
- POVIDONE, UNSPECIFIED
- STEARIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68071-3883 | 68071-3883-2 |
| 0113-0403 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
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 |
|---|---|---|---|---|---|---|
| good sense pain relief | ACETAMINOPHEN | NuCare Pharmaceuticals,Inc. | 3c1f505d-0319-a179-e063-6294a90a0b17 | 2025-08-11 | Warnings | 68071-3883-2 68071-3883 68071388302 3c1f4cef-f586-d95b-e063-6394a90a4d4b 3c1f505d-0319-a179-e063-6294a90a0b17 |
| good sense pain relief | ACETAMINOPHEN | L. Perrigo Company | 8b56bfc0-2253-458d-99a6-0b0f9ae0ba50 | 2024-10-21 | Warnings | 0113-0403 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.