CHILDRENS IBUPROFEN- ibuprofen suspension 
Chain Drug Marketing Association, Inc.

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Children's Ibuprofen Oral Suspension

Drug Facts

Active ingredient
(in each 5 mL)
Ibuprofen 100 mg (NSAlD)*
*nonsteroidal anti-inflammatory drug

Purpose
Ibuprofen .... 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 asevere 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
NSAID, 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: NSAIDs, 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 11years 15 mL

* or as directed by a doctor

Other information
■ each 5 mL contains: sodium 2 mg
■ store between 20-25ºC (68-77ºF)
■ do not use if carton is opened or printed bottle
  neckband is broken or missing
■ see bottom panel for lot number and expiration date

Inactive ingredients
Acesulfame potassium, anhydrous citric acid,
carboxymethylcellulose sodium, D&C Yellow #10, FD&C
Red #40, flavors, glycerin, microcrystalline cellulose,
polysorbate 80, propylene glycol, purified water, sodium
benzoate, sucrose, and xanthan gum

Questions or comments?
Call 732-314-4550 from 9AM to SPM EST,
Monday - Friday.

children's

ibuprofen

Oral  Suspension (NSAID)

For Ages 2 to 11 Years

                                             NDC 63868-795-04

QC

QUALITY CHOICE        See New Warnings

Compare to the
active ingredient in
Children's Motrin​®

children's
ibuprofen

Oral Suspension (NSAID)
100 mg per 5 mL

Pain Reliever/Fever Reducer

8 HRS    Lasts up to
              8 Hours

For ages 2 to 11 years
Alcohol Free

Original Berry
Flavor

4 fl oz (118 mL)

Important: Read all product indormation 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®.

BX-117

Distributed by C.D.M.A., Inc.©
43157 W 9 Mile Rd
Novi, MI 48375
www.qualitychoice.com
Questions: 800-935-2362

4 OZ

Berry 795-04 4OZBerry 795-04 4OZ

8 OZ

Berry 795-08 8OZBerry 795-08 8OZBerry 795-08 8OZ

res

CHILDRENS IBUPROFEN 
ibuprofen suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-795
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 YELLOW NO. 10 (UNII: 35SW5USQ3G)  
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
ColororangeScore    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-795-041 in 1 CARTON12/15/2020
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:63868-795-081 in 1 CARTON12/15/2020
2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21060212/15/2020
Labeler - Chain Drug Marketing Association, Inc. (011920774)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(63868-795)

Revised: 12/2023
Document Id: 28940dbe-2b8d-466d-a1c0-af9377be11f1
Set id: afbfb065-8f84-4781-babd-f4225fbdad6e
Version: 4
Effective Time: 20231230
 
Chain Drug Marketing Association, Inc.