Ibuprofen by Bryant Ranch Prepack IBUPROFEN tablet

Ibuprofen by

Drug Labeling and Warnings

Ibuprofen by is a Otc medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Ibuprofen 200 mg (NSAID)*

*nonsteroidal anti- inflammatory drug 

Purpose

Pain Reliever/ Fever Reducer

Uses

temporarily relieves minor aches and pain due to:

• headache
• toothache
• backache
• menstrual cramps
• the common cold
• muscular aches
• minor pain of arthritis
• temporarily 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 NSAID, which may cause severe stomach bleeding. The chance is higher if you

• are age 60 or older
• have had stomach ulcers or bleeding problems
• take a blood thinning (anticoagulant) or steroid drug
• take other drugs containing prescription or non prescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
• have 3 or more alcoholic drinks everyday while using this product
• take more or for a longer time than directed

Do not use

• if you have ever had an allergic reaction to any other pain reliever/ fever reducer
  
• right before or after heart surgery
  

Ask a doctor before use if

• stomach bleeding warning applies to you
• you have problems or serious side effects from taking pain relievers or fever reducers
• you have a history of stomach problems, such as heartburn
• you have high blood pressure, heart disease, liver cirrhosis, kidney disease or asthma
• you are taking a diuretic
  

Ask a doctor or pharmacist before use if you are

• under a doctor's care for any serious condition
• taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
  
• taking any other drug
  

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

Stop use and ask a doctor if

• you experience any of the following signs of stomach bleeding:
• feel faint
• vomit blood
• have bloody or black stools
• have stomach pain that does not get better
• pain gets worse or last for more than 10 days
• fever gets worse or last more than 3 days
• redness or swelling is present in the painful area
• any new symptoms appear

If pregnant or breast feeding,

ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

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). This Package for Households Without Young Children.

Directions

• do not take more than directed

• the smallest effective dose should be used

• adults and children 12 years and older:
  • take 1 tablet every4 to 6 hours while symptoms persist
  • if pain or fever does not respond to 1 tablet, 2 tablets may be used
  • do not exceed 6 tablets in 24 hours, unless directed by a doctor
• children under 12 years:
  • consult a doctor

Other information

• Tamper Evident: do not use if safety seal under cap is broken or missing
• store at room temperature (20o- 25oC) 
• avoid excessive heat above 40oC (104oF)

Inactive Ingredients:

colloidal silicon dioxide, croscarmellose sodium, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, red iron oxide, talc & titanium dioxide  

Questions? Adverse drug event call: (800)687-0176 Mon-Fri: 8 AM to 4 PM

*This product is not manufactured or distributed by Pfizer Consumer Products, owner of the registered trademark ADVIL®.

HOW SUPPLIED

Product: 71335-0223

NDC: 71335-0223-5 60 TABLET in a BOTTLE

NDC: 71335-0223-8 10 TABLET in a BOTTLE

NDC: 71335-0223-2 15 TABLET in a BOTTLE

NDC: 71335-0223-3 30 TABLET in a BOTTLE

NDC: 71335-0223-0 90 TABLET in a BOTTLE

NDC: 71335-0223-9 56 TABLET in a BOTTLE

NDC: 71335-0223-6 50 TABLET in a BOTTLE

NDC: 71335-0223-7 40 TABLET in a BOTTLE

NDC: 71335-0223-1 20 TABLET in a BOTTLE

NDC: 71335-0223-4 100 TABLET in a BOTTLE

Ibuprofen 200mg Tablet

INGREDIENTS AND APPEARANCE

IBUPROFEN 
ibuprofen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71335-0223(NDC:66424-396)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM)	IBUPROFEN	200 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
STARCH, CORN (UNII: O8232NY3SJ)
FERRIC OXIDE RED (UNII: 1K09F3G675)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	brown	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	114
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-0223-5	60 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
2	NDC: 71335-0223-8	10 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
3	NDC: 71335-0223-2	15 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
4	NDC: 71335-0223-3	30 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
5	NDC: 71335-0223-0	90 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
6	NDC: 71335-0223-9	56 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
7	NDC: 71335-0223-6	50 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
8	NDC: 71335-0223-7	40 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
9	NDC: 71335-0223-1	20 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016
10	NDC: 71335-0223-4	100 in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091239	03/01/2016

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-0223) , RELABEL(71335-0223)