CHILDRENS IBUPROFEN ORAL SUSPENSION, BUBBLE GUM- ibuprofen suspension 
Best Choice

----------

Children's Ibuprofen Oral Suspension, Bubble Gum Flavor

Drug Facts

Active ingredient
(in each 5 mL)

Ibuprofen 100 mg (NSAID)*
*nonsteroidal anti-inflammatory drug

Purpose
Pain reliever/
fever reducer

Uses temporarily:

■ relieves minor aches and pains due to the common cold,
   flu, sore throat, headache and toothache

■ reduces fever

Warnings
Allergy alert: Ibuprofen may cause a severe allergic
reaction, especially in people allergic to aspirin. Symptoms
may include: 
   ■ hives  ■ facial swelling  ■asthma (wheezing)
   ■ shock ■ skin reddening  ■ rash
   ■ blisters
If an allergic reaction occurs, stop use and seek medical
help right away.
Stomach bleeding warning: This product contains an
NSAlD, which may cause severe stomach bleeding. The
chance is higher if your child:
■ has had stomach ulcers or bleeding problems
■ takes a blood thinning (anticoagulant) or steroid drug
■ takes other drugs containing prescription or
   nonprescription NSAIDs (aspirin, ibuprofen,
   naproxen, or others)
■ takes more or for a longer time than directed
Heart attack and stroke warning: NSAlDs, except
aspirin, increase the risk of heart attack, heart failure, and
stroke. These can be fatal. The risk is higher if you use
more than directed or for longer than directed.
Sore throat warning: Severe or persistent sore throat or
sore throat accompanied by high fever, headache, nausea,
and vomiting may be serious. Consult doctor promptly. Do
not use more than 2 days or administer to children under 3
years of age unless directed by doctor.

Do not use
■ If the child has ever had an allergic reaction to Ibuprofen
   or any other pain reliever/fever reducer
■ right before or after heart surgery

Ask a doctor before use if
■ stomach bleeding warning applies to your child
■ child has a history of stomach problems, such as
   heartburn
■ child has problems or serious side effects from taking
   pain relievers or fever reducers
■ child has not been drinking fluids
■ child has lost a lot of fluid due to vomiting or diarrhea
■ child has high blood pressure, heart disease, liver
  cirrhosis, kidney disease, or had a stroke
■ child has asthma
■ child is taking a diuretic

Ask a doctor or pharmacist before use if the child is
■ under a doctor's care for any serious condition
■ taking any other drug

When using this product
■ take with food or milk if stomach upset occurs

Stop use and ask a doctor if
■ child experiences any of the following signs of
  stomach bleeding:
  ■ feels faint             ■ vomits blood
  ■ has bloody or black stools
  ■ has stomach pain that does not get better
■ child has symptoms of heart problems or stroke:
  ■ chest pain            ■ trouble breathing
  ■ weakness in one part or side of body
  ■ slurred speech      ■ leg swelling
■ the child does not get any relief within first day
  (24 hours) of treatment
■ fever or pain gets worse or lasts more than 3 days
■ redness or swelling is present in the painful area
■ any new symptoms appear

Keep out of reach of children. In case of overdose, get
medical help or contact a Poison Control Center right
away. (1-800-222-1222)

Directions
this product does not contain directions or
   complete warnings for adult use
do not give more than directed
■ shake well before using
■ mL= milliliter
■ find right dose on chart. If possible, use weight to
   dose; otherwise use age.
■ use only enclosed dosing cup. Do not use any other
   dosing device.
■ if needed, repeat dose every 6-8 hours
■ do not use more than 4 times a day
■ replace original bottle cap to maintain child resistance

                                       Dosing Chart

 Weight (lb)Age (yr)Dose (mL)*
 under 24 under 2 years ask a doctor
 24-35 lbs 2-3 years 5 mL
 36-47 lbs 4-5 years 7.5 mL
 48-59 lbs 6-8 years 10 mL
 60-71 lbs 9-10 years 12.5 mL
 72-95 lbs 11 years

 15 mL

*or as directed by a doctor

Other information
■ each 5 mL contains: sodium 2 mg
■ store between 20-25° C (68-77° F)
■ do not use if printed neckband is broken or missing

Inactive ingredients
Acesulfame potassium, anhydrous citric acid,
carboxymethylcellulose sodium, D&C Red #33, FD&C Red
#40, flavors, glycerin, microcrystalline cellulose, polysorbate
80, propylene glycol, purified water, sodium benzoate,
sucrose, and xanthan gum

Questions or comments?
Call weekdays from 9:30 AM to 4:30 PM EST at
1-732-314-4550

--------------

Package Labeling: Best Choice® Children's Ibuprofen Oral Suspension, Bubble Gum Flavor

Best Choice​®

Children's

Ibuprofen

Oral Suspension (NSAID)

100 mg per 5 ml

Pain Reliever/Fever Reducer

COMPARE TO THE

ACTIVE INGREDIENT

IN CHILDREN'S

MOTRIN®**

LASTS UP TO

8 HOURS

For ages

2 to 11 years

Bubble Gum Flavor

4 FL OZ (118 mL)

Important Read all product information before using.
Keep this box for important information.
This product is intended for use in children.

**This product is not manufactured or distributed by McNeil

Consumer Healthcare, distributor of Children's Motrin®

PROUDLY DISTRIBUTED BY:

VALUE MERCHANDISERS, CO.

5000 KANSAS AVE

KANSAS CITY, KS 66106

Carton

127-24 BublGum Crtn

Bottle

127-24 BublGum Botl

res

CHILDRENS IBUPROFEN ORAL SUSPENSION, BUBBLE GUM 
ibuprofen suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-127
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorpinkScore    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63941-127-241 in 1 CARTON01/01/2025
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21060201/01/2025
Labeler - Best Choice (868703513)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(63941-127)

Revised: 1/2025
Document Id: 77ca4e17-f27e-4933-9f27-7087cd616fec
Set id: d27ca801-d4d3-4fd0-a22b-db5ada5fcb9f
Version: 1
Effective Time: 20250120
 
Best Choice