Indications and uses
• temporarily relieves minor aches and pains due to: • the common cold • headache • backache • minor pain of arthritis • toothache • muscular aches • premenstrual and menstrual cramps • temporarily reduces fever
Acetaminophen Tablets 500 mg
- Manufacturer
- NuCare Pharmaceuticals, Inc.
- Effective date
- 2026-06-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-06-16 05:10:29
Label at a glance#
ProductACETAMINOPHEN
Active ingredientACETAMINOPHEN
Label structure15 sections
Dosage and administration
• do not take more than directed (see overdose warning) adults and children 12 years and over • take 2 caplets every 6 hours while symptoms last • do not take more than 6 caplets 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
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENT (IN EACH CAPLET)
Acetaminophen, USP 500 mg
PURPOSE
Pain reliever/fever reducer
USES
• temporarily relieves minor aches and pains due to:
• the common cold
• headache
• backache
• minor pain of arthritis
• toothache
• muscular aches
• premenstrual and menstrual cramps
• temporarily reduces fever
WARNINGS
Liver warning:This product contains acetaminophen. Severe Liver damage may occur if you take
• more than 4,000 mg of acetaminophen 24 hours.
• with other drugs containing acetaminophen
• 3 or more alcoholic drinks everyday 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 drugs 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 other inactive ingredients in this product.
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 doctor if
• pain gets worse or lasts more than 10 days
• fever gets worse or lasts more than 3 days
• new symptoms 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.
Keep out of reach of children
Over dose warning: In case of overdose, get medical help or Contact 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 | • take 2 caplets every 6 hours while symptoms last
• do not take more than 6 caplets 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 INFORMATION
•store at 20-25°C (68-77°F). See USP Controlled Room Temparature
•avoid high humidity
•See end panel for lot number and expiration date
INACTIVE INGREDIENTS
hydroxyethyl methyl cellulose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid.
QUESTIONS OR COMMENTS ?
Contact 1-877-770-3183Mon-Fri 8:00 AM EST to 5:00 PM PST.
+All trademarkes are property of their reapective owners.
This product is not affliated with the makers/owners of
Extra Strength Tylenol ®Caplets.
Distributed by:
Granules Pharmaceuticals INc.,
Chantilly, VA 20151
MADE IN INDIA
Rev.08/21
PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Data Matrix | 0100368071530049210000000002<GS>170000010000000<GS> | 68071-5300-4.jpg |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70010-161-01 | EA - Each | 70010-161 | 0ed1eb5c-3333-4e86-b023-551784d2efd3 | 1 | 2023-08-08 |
| 70010-161-05 | EA - Each | 70010-161 | 2e1e4e0f-4cc6-437a-aa64-bf9985bbf911 | 1 | 2023-08-08 |
| 70010-161-10 | EA - Each | 70010-161 | 70fddc44-fb63-4964-a389-6514804206a8 | 1 | 2024-02-14 |
Products#
Every source-derived product name is available through these pages.
- ACETAMINOPHEN
- POVIDONE K30
- STARCH, CORN
- STEARIC ACID
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL 400
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68071-5300 | 68071-5300-4 |
| 70010-161 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POVIDONE K30 | U725QWY32X | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| POLYETHYLENE GLYCOL 400 | B697894SGQ | 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 |
|---|---|---|---|---|---|---|
| ACETAMINOPHEN | ACETAMINOPHEN | NuCare Pharmaceuticals, Inc. | 54010ddf-25d1-2016-e063-6294a90a877d | 2026-06-11 | Warnings | 68071-5300-4 68071-5300 68071530004 54010ddf-25d2-2016-e063-6294a90a877d 54010ddf-25d1-2016-e063-6294a90a877d |
| ACETAMINOPHEN | ACETAMINOPHEN | Granules Pharmaceuticals Inc. | d5d49146-665e-4a93-e053-2995a90aca59 | 2025-04-02 | Warnings | 70010-161 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.