CHILDRENS ACETAMINOPHEN- acetaminophen suspension 
Cardinal Health 107, LLC

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Children's Acetaminophen Oral Suspension
Ibuprofen Free/Alcohol Free/Aspirin Free

Drug Facts

Active ingredient                                                                                 
(in each 5 mL)  

Acetaminophen 160 mg

Purpose

Pain reliever/fever reducer

Uses

temporarily:

reduces fever
relieves minor aches and pain due to:
the common cold
flu
headache
sore throat
toothache

Warnings

Liver warning: This product contains 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.
• if your child is allergic to acetaminophen or any of the inactive ingredients in this product.

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.

When using this product, do not exceed the recommended dose (see overdose warning)

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
• new symptoms occur
• redness or swelling is present


These could be signs of a serious condition.

Keep out of the 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 children even if you do not notice any sign or symptoms

Directions

this product does not contain directions or complete warnings for adult use
do not take more than directed (see overdose warning)
shake well before using
mL = milliliter
find the right dose on chart below. If possible, use weight to dose; otherwise, use age
repeat dose every 4 hours while symptoms last
do not give more than 5 times in 24 hours
*
or as directed by a doctor

Weight (lbs)

Age (yr)

Dose (mL) *

Under 24

Under 2

Ask a doctor

24-35

2-3 years

5 mL 

36-47

4-5 years

7.5 mL 

48-59

6-8 years

10 mL 

60-71

9-10 years

12.5 mL 

72-95

11 years

15 mL 

Other information

each 5 mL contains: sodium 2 mg
Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]
protect from freezing
a red, berry flavored suspension supplied in the following oral dosage form:

Overbagged with 5 Unit-Dose Cups per bag, NDC 55154-5787-5

Inactive ingredients

Acesulfame K, butylparaben, citric acid, FD&C Red No. 40, flavoring, glycerin, high fructose corn syrup, polysorbate 80, propylene glycol, purified water, sodium benzoate, sorbitol solution, veegum and xanthan gum.

Questions or comments?

Call 1-800-845-8210.

MANUFACTURED BY

Pharmaceutical Associates, Inc.

Greenville, SC 29605

www.paipharma.com

Distributed By:

Cardinal Health

Dublin, OH 43017

L55345731223

R09/20

PRINCIPAL DISPLAY PANEL - 5 mL Cup

Children’s Acetaminophen Oral Suspension

160 mg per 5 mL

5 Unit-Dose Cups

Bag Label
CHILDRENS ACETAMINOPHEN 
acetaminophen suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-5787(NDC:0121-1781)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN160 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-5787-55 in 1 BAG09/17/2007
15 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01309/17/2007
Labeler - Cardinal Health 107, LLC (118546603)

Revised: 1/2024
Document Id: 5842dbe0-08b2-4363-82f8-9de5e854d1bf
Set id: 7562f4e4-54fa-488c-a199-48ad2632e2a1
Version: 7
Effective Time: 20240105
 
Cardinal Health 107, LLC