CHILDRENS PAIN RELIEF- childrens pain relief liquid 
Allegiant Health

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455 - Children Pain Relief Oral Suspension

Active ingredient(s)

Acetaminophen 160 mg 

(in each 5 mL = 1 teaspoonful)

Purpose

Pain reliever/fever reducer

Use(s)

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

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 ever, 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 other 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 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 ■ redness or swelling is present. These could be signs of a serious condition.

Keep out of reach of children

Overdose warning: Taking more than the recommended dose (overdose) may
cause liver damage. In case of overdose, get medical help or contact a Poison
Control Center (1-800-222-1222) 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

■ this product does not contain directions or complete warnings for adult use.■ shake well before using

■ mL = milliliter; tsp = teaspoonful ■ find the right dose on the chart below. If possible, use weight to dose, otherwise, use age.

■ if needed, repeat dose every 4 hours while symptoms last ■ do not give more than 5 times in 24 hours

■ do not give for more than 5 days unless directed by a doctor

Weight (lb)Age (yr)Dose (mL)*

under 24

under 2 years

ask a doctor

24-35

2-3 years

5 mL(1 tsp)

36-47

4-5 years

7.5 mL(1 1/2 tsp)

48-59

6-8 years

10 mL(2 tsp)

60-71

9-10 years

12.5 mL(2 1/2 tsp)

72-95

11 years

15 mL(3 tsp)

*or as directed by a doctor

Attention: use only enclosed dosing cup specifically designed for use with this
product. Do not use any other dosing device.

Other information

■ each 5 mL (1 tsp) contains; sodium 3 mg ■ store between 20-25ºC (68-77ºF) ■ do not refrigerate ■ Keep carton for full directions for use.

Inactive ingredients

anhydrous citric acid, butylparaben, FD&C red
#40, flavor, glycerin, high fructose corn syrup, microcrystalline cellulose and
carboxymethylcellulose sodium, propylene glycol, purified water, sodium
benzoate, sorbitol solution, sucralose, xanthan gum

Questions/Comments

Call 1-888-952-0050 Monday through Friday 9AM - 5PM EST

Principal Display Panel

Pain Relief

Pain Relief

CHILDRENS PAIN RELIEF 
childrens pain relief liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-455
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
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL SOLUTION (UNII: 8KW3E207O2)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69168-455-531 in 1 CARTON04/11/2024
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01304/11/2024
Labeler - Allegiant Health (079501930)

Revised: 4/2024
Document Id: c7cb6d3f-70c7-4105-bf23-f17e220d1445
Set id: 7381dd26-c507-4d02-b989-cfd96e02f495
Version: 2
Effective Time: 20240411
 
Allegiant Health