IBUPROFEN PAIN RELIEVER/ FEVER REDUCER- ibuprofen suspension 
Amneal Pharmaceuticals

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Ibuprofen Oral Suspension, USP (NSAID)
Pain Reliever/ Fever Reducer
100 mg/ 5 mL

OTC - ACTIVE INGREDIENT

Active Ingredient                               

(in each 5 mL = 1 teaspoon)

Ibuprofen 100 mg (NSAID)*

*nonsteroidal anti-inflammatory drug

OTC - PURPOSE

Purpose

Pain reliever/ fever reducer

INDICATIONS AND USAGE

Uses

Temporarily:

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

■ Reduces fever

WARNINGS

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 a nonsteroidal anti-inflammatory drug (NSAID), which may cause severe stomach bleeding. The chances are higher if your child:

■ has had stomach ulcers or bleeding problems

■ takes a blood thinning (anticoagulant) or steroid drug

■ takes other drugs containing an NSAID (aspirin, ibuprofen, naproxen, or others)

■ takes more or for a longer time 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.

OTC - DO NOT USE

Do not use:

■ if the child has ever had an allergic reaction to any other pain reliever/fever reducer

■ right before or after heart surgery

OTC - ASK DOCTOR

Ask a doctor before use if:

■ child has problems or serious side effects from taking pain relievers or fever reducers

■ stomach bleeding warning applies to your child

■ child has a history of stomach problems, such as heartburn

■ 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, or kidney disease

■ child has asthma

■ child is taking a diuretic

OTC - ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if the child is:

■ under doctor’s care for any serious condition

■ taking any other drug

OTC - WHEN USING

When using this product:

■ take with food or milk if stomach upset occurs

■ the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

OTC - STOP USE

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

■ the child does not get any relief within the 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

OTC - KEEP OUT OF REACH OF CHILDREN

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)

DOSAGE AND ADMINISTRATION

Directions

this product does not contain directions or complete warnings for adult use

do not give more than directed

■ shake well before using

■ find right dose on chart below (if possible, use weight to dose; otherwise use age)

■ use only enclosed measuring cup

■ 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 (tsp or mL)
under 2 years ask a doctor
24-35 lbs2-3 years1 tsp or 5 mL
36-47 lbs4-5 years1 ½ tsp or 7.5 mL
48-59 lbs6-8 years2 tsp or 10 mL
60-71 lbs9-10 years2 ½ tsp or 12.5 mL
72-95 lbs11 years3 tsp or 15 mL

OTHER INFORMATION

Other information

■ each teaspoon contains: sodium 2 mg

■ store between 20° to 25°C (68° to 77°F)

■ do not use if bottle wrap, or imprinted foil inner seal is broken or missing

■ see bottom panel for lot number and expiration date

INACTIVE INGREDIENTS

acesulfame-potassium, anhydrous citric acid, D&C yellow # 10, FD&C red # 40, glycerin, NA bubble gum flavor FQ5511, polysorbate 80 (tween 80), purified water, sodium benzoate, sucrose, xanthan gum

OTC - QUESTIONS

Questions or Comments? Call 1-877-835-5472,

Monday through Friday 9AM - 5PM EST.

Keep the carton.

It contains important information.

See end panel for expiration date.

*This product is not manufactured or distributed by McNeil-PPC, Inc., distributor of Children’s Motrin®.

Distributed by: Amneal Pharmaceuticals

Glasgow, KY 42141

Rev. 07-2011

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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IBUPROFEN  PAIN RELIEVER/ FEVER REDUCER
ibuprofen suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65162-672
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)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorORANGEScore    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65162-672-861 in 1 CARTON
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20045711/12/2011
Labeler - Amneal Pharmaceuticals (123797875)
Registrant - Amneal Pharmaceuticals (123797875)
Establishment
NameAddressID/FEIBusiness Operations
Amneal Pharmaceuticals968119730ANALYSIS, MANUFACTURE, LABEL, PACK

Revised: 2/2012
Document Id: 010ab916-bc42-4e69-85d6-6585fc34226d
Set id: ae1cb9ae-9d01-47f0-b9ec-0d924d913514
Version: 4
Effective Time: 20120221
 
Amneal Pharmaceuticals