Childrens Ibuprofen description, usages, side effects, indications, overdosage, supplying and lots more!

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Childrens Ibuprofen

Precision Dose Inc.

CHILDREN'S IBUPROFEN ORAL SUSPENSION Berry Flavor


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

100 mg/5 mL   200 mg/10 mL

For Hospital Use Only

Drug Facts

Active Ingredient (in each 5 mL = 1 teaspoonful)

Ibuprofen 100 mg (NSAID)nonsteroidal anti-inflammatory drug

Purposes

Pain reliever/Fever reducer

Childrens Ibuprofen Uses

temporarily:

  • relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache
  • reduces fever
  • This product is intended for use in children.

Warnings

Allergy alert

Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

  • hives
  • asthma (wheezing)
  • skin reddening
  • facial swelling
  • shock
  • 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

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 any other pain reliever/fever reducer
  • right before or after heart surgery

Ask a doctor before use if

  • the 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, or kidney disease
  • 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

  • give 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

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 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

  • use as directed per healthcare professional
  • this product does not contain directions or complete warnings for adult use
  • do not give more than directed
  • shake cups well before using
  • if needed, repeat dose every 6 - 8 hours
  • do not use more than 4 times a day

Other Information

  • each teaspoon contains: sodium 2 mg
  • store at 20-25°C (68-77°F)
  • See individual label or shipper label for lot number and expiration date.

Inactive Ingredients

anhydrous citric acid, artificial mixed berry flavor, D&C yellow #10, FD&C red #40, glycerin, high fructose corn syrup, hypromellose, polysorbate 80, purified water, sodium benzoate, sorbitol solution, xanthan gum

Alcohol Free, Gluten Free

How Supplied

NDC 68094-494-58
5 mL per unit dose syringe
Fifty (50) unit dose syringes per shipper

NDC 68094-494-61
5 mL per unit dose cup
One hundred (100) cups per shipper

NDC 68094-494-62
5 mL per unit dose cup
Thirty (30) cups per shipper

NDC 68094-503-61
10 mL per unit dose cup
One hundred (100) cups per shipper

NDC 68094-503-62
10 mL per unit dose cup
Thirty (30) cups per shipper

Manufactured By:
Perrigo Company
515 Eastern Avenue
Allegan, MI 49010

Packaged By:
Precision Dose, Inc.
722 Progressive Lane
S. Beloit, IL 61080

LI 587
Rev. 04/11

PRINCIPAL DISPLAY PANEL - 5 mL Cup Label

NDC# 68094-494-58

Children's IBUPROFEN Oral Suspension, 100 mg/5 mL

Delivers 5 mL
(NSAID)
For Hospital Use Only

Each 5 mL contains: sodium 2 mg

Alcohol Free
Gluten Free

Store at 20°-25°C (68°-77°F)
Protect from freezing

Pkg: Precision Dose, Inc. S. Beloit, IL 61080

LSY495 Rev. 04/11

For Oral Use Only

Childrens Ibuprofen

PRINCIPAL DISPLAY PANEL - 200 mg/10 mL Lid

NDC 68094-503-59

PrecisionDose™

Children's IBUPROFEN
Oral Suspension
200 mg/10 mL

Delivers 10 mL Shake Well (NSAID) Alcohol Free Gluten Free
Each 5 mL contains: sodium 2 mg

Hospital Use Only
Store at 20-25°C (68-77°F)
Pkg. By: Precision Dose, Inc.
S. Beloit, IL 61080

Childrens Ibuprofen

Childrens Ibuprofen

Ibuprofen SUSPENSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68094-494(NDC:0113-0897)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
IBUPROFEN IBUPROFEN 100 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS CITRIC ACID
D&C YELLOW NO. 10
FD&C RED NO. 40
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
HYPROMELLOSES
polysorbate 80
water
SODIUM BENZOATE
sorbitol
XANTHAN GUM

Product Characteristics

Color
ORANGE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68094-494-59 5 in 1 CUP, UNIT-DOSE
2 NDC:68094-494-59 5 in 1 CUP, UNIT-DOSE
3 5 in 1 SYRINGE
4 10 in 1 BAG
5 NDC:68094-494-58 5 in 1 CASE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074937 2004-04-13


Childrens Ibuprofen

Ibuprofen SUSPENSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68094-503(NDC:0113-0897)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
IBUPROFEN IBUPROFEN 200 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS CITRIC ACID
D&C YELLOW NO. 10
FD&C RED NO. 40
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
HYPROMELLOSES
polysorbate 80
water
SODIUM BENZOATE
sorbitol
XANTHAN GUM

Product Characteristics

Color
ORANGE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68094-503-59 10 in 1 CUP, UNIT-DOSE
2 NDC:68094-503-59 10 in 1 CUP, UNIT-DOSE
3 10 in 1 TRAY
4 NDC:68094-503-61 10 in 1 CASE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074937 2006-09-14


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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