Indications and uses
temporarily relieves minor aches and pains temporarily reduces fever
155-gcp
- Manufacturer
- Geri-Care Pharmaceutical Corp
- Effective date
- 2026-09-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- daily-update
- Hydrated at
- 2026-09-15 03:01:29
Label at a glance#
ProductChildrens Acetaminophen
Active ingredientACETAMINOPHEN
Label structure9 sections
Dosage and administration
this product does not contain directions or complete warnings for adult use do not give more than directed find the right dose on chart below. If possible, use weight to dose; otherwise, use age. chew or crush tablets completely before swallowing; do not swallow tablets whole repeat dose every 4 hours while symptoms last do not give more than 5 times in 24 hours Weight (lb) Age (yr) Dose (chewable tablets)* Under ...
Storage and handling
store at 20-25°C (68-77°F); excursions permitted between 15°-30°C (59°-86°F) avoid high humidity
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each chewable tablet)
Acetaminophen 160 mg
Purpose
Pain reliever/fever reducer
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Warnings
Liver warning:This product contains acetaminophen. Severe liver damage may occur if your child takes
- more than 5 doses in 24 hours, which is the maximum daily amount
- with other drugs containing acetaminophen
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.
Sore throat warning:If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
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 your child has
liver disease.
Ask a doctor or pharmacist before use if your child is
taking the blood thinning drug warfarin.
Stop use and ask a doctor if
- pain gets worse or lasts more than 5 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present
- any new symptoms appear
These could be signs of a serious condition.
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.
Directions
- this product does not contain directions or complete warnings for adult use
- do not give more than directed
- find the right dose on chart below. If possible, use weight to dose; otherwise, use age.
- chew or crush tablets completely before swallowing; do not swallow tablets whole
- repeat dose every 4 hours while symptoms last
- do not give more than 5 times in 24 hours
| Weight (lb) | Age (yr) | Dose (chewable tablets)* |
| Under 24
| Under 2
| Ask a doctor
|
| 24-35
| 2-3
| 1 tablet
|
| 36-47
| 4-5
| 1 1/2 tablets
|
| 48-59
| 6-8
| 2 tablets
|
| 60-71
| 9-10
| 2 1/2 tablets
|
| 72-95
| 11
| 3 tablets
|
*or as directed by a doctor
Other information
- store at 20-25°C (68-77°F); excursions permitted between 15°-30°C (59°-86°F)
- avoid high humidity
Inactive ingredients
citric acid, crospovidone, D&C red #27 aluminum lake, D&C red #30 aluminum lake, dextrates hydrated, ethylcellulose, FD&C blue #1 aluminum lake, flavors, magnesium stearate, mannitol, polyethylene, stearic acid, sucralose
Questions or comments?
1-800-540-3765
Principal display panel
Childrens Chewable
Acetaminophen 160 mg
Products#
Every source-derived product name is available through these pages.
- Childrens Acetaminophen
- Acetaminophen
- CITRIC ACID MONOHYDRATE
- CROSPOVIDONE, UNSPECIFIED
- D&C RED NO. 27 ALUMINUM LAKE
- D&C RED NO. 30 ALUMINUM LAKE
- DEXTROSE MONOHYDRATE
- ETHYLCELLULOSE, UNSPECIFIED
- FD&C BLUE NO. 1 ALUMINUM LAKE
- MAGNESIUM STEARATE
- MANNITOL
- HIGH DENSITY POLYETHYLENE
- STEARIC ACID
- SUCRALOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57896-155 | 57896-155-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.