Indications and uses
temporarily relieves minor aches and pains temporarily reduces fever
Regular Strength Pain Relief
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2021-03-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:38:40
Label at a glance#
ProductRegular Strength Pain Relief
Active ingredientACETAMINOPHEN
Label structure9 sections
Dosage and administration
do not take more than directed adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 10 tablets in 24 hours children under 12 years: ask a doctor
Storage and handling
store at 20⁰C-25⁰C (68⁰F-77⁰F)
Label contents#
Full prescribing information#
Active Ingredients
Acetaminophen 325 mg
Purpose
Pain Reliever/Fever Reducer
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Warnings
Liver warning: This product contains acetaminophen.
The maximum daily dose of this product is 10 tablets
in 24 hours. Severe liver damage may occur if you take:
- more than 12 tablets (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.
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.
Ask a doctor before use if you have liver disease
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
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 symptom occur
- redness or swelling is present
These could be signs of a serious condition.
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. In case of overdose, get
medical help or contact a Poison Control Center right away.
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
- adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 10 tablets in 24 hours
- children under 12 years: ask a doctor
Other Information
- store at 20⁰C-25⁰C (68⁰F-77⁰F)
Inactive Ingredients
povidone, sodium starch glycolate, starch stearic acid.
HOW SUPPLIED
Product: 50090-5148
NDC: 50090-5148-2 100 TABLET in a BOTTLE
NDC: 50090-5148-3 30 TABLET in a BOTTLE
Acetaminophen
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50090-5148-2 | 2023-01-30 | C162847 | 48780-1 | f386c649-a81e-0266-e053-dadaa90a7c1a | gc 102 |
| 50090-5148-3 | 2023-01-30 | C162847 | 48780-1 | f386c649-a81e-0266-e053-dadaa90a7c1a | gc 102 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-5148-2 | Regular Strength Pain Relief | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 50090-5148-3 | Regular Strength Pain Relief | 30 in 1 BOTTLE | TABLET | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-5148 | REGULAR STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210303_287a8522-ec1f-4322-bfd0-d707dcb430c7.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-102-01 | EA - Each | 57896-102 | 4fd0e2b7-fd19-4784-9e24-f0fc69b74910 | 1 | 2019-01-24 |
| 57896-102-05 | EA - Each | 57896-102 | b63010e7-a608-44c2-b043-44d6f2818c59 | 1 | 2019-02-13 |
| 57896-102-10 | EA - Each | 57896-102 | 6b3d573d-baa1-4daf-aba9-717aa1dcfc74 | 1 | 2019-02-13 |
| 57896-102-20 | EA - Each | 57896-102 | 40b6eab0-c1a1-4c63-82f8-78251de158a2 | 1 | 2021-12-08 |
Products#
Every source-derived product name is available through these pages.
- Regular Strength Pain Relief
- Acetaminophen
- POVIDONE, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STARCH, CORN
- STEARIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50090-5148 | 50090-5148-2, 50090-5148-3 |
| 57896-102 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
| STARCH, CORN | O8232NY3SJ | 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 |
|---|---|---|---|---|---|---|
| Regular Strength Pain Relief | ACETAMINOPHEN | Geri-Care Pharmaceutical Corp | 6158e954-32d8-4718-e053-2a91aa0a27f3 | 2024-12-31 | Warnings | 57896-102 |
| 405475f5-3a52-4228-9999-dd0a7be02e1c | 287a8522-ec1f-4322-bfd0-d707dcb430c7 | 2021-03-02 | Warnings | 405475f5-3a52-4228-9999-dd0a7be02e1c 287a8522-ec1f-4322-bfd0-d707dcb430c7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.