DailyMed - UP AND UP IBUPROFEN- ibuprofen tablet, film coated

NDC Code(s): 11673-517-78
Packager: Target Corporation

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated August 29, 2023

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Active ingredient (in each caplet)
Ibuprofen 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug

Ibuprofen 200 mg (NSAID)*

*nonsteroidal anti-inflammatory drug
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Purposes
Pain reliever/fever reducer

Pain reliever/fever reducer
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Uses
• temporarily relieves minor aches and pains due to: • headache - • muscular aches - • minor pain of arthritis - • toothache - • backache - • the common cold - • menstrual cramps - • temporarily reduces ...

•

temporarily relieves minor aches and pains due to:

•

headache

•

muscular aches

•

minor pain of arthritis

•

toothache

•

backache

•

the common cold

•

menstrual cramps

•

temporarily reduces fever

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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 ...

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 nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]

•

have 3 or more alcoholic drinks every day while using this product

•

take more or for a longer time than directed

Heart attack and warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stoke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use

•

if you have 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

•

you have problems or serious side effects from taking pain relievers or fever reducers

•

the stomach bleeding warning applies to you

•

you have a history of stomach problems, such as heartburn

•

you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke

•

you are taking a diuretic

Ask a doctor or pharmacist before use if you are

•

taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin

•

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

•

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

•

you have symptoms of heart problems or stroke:

•

chest pain

•

trouble breathing

•

weakness in one part or side of body

•

slurred speech

•

leg swelling

•

pain gets worse or lasts more than 10 days

•

fever gets worse or lasts 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 at 20 weeks or later in 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).

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Directions

• do not take more than directed - • the smallest effective dose should be used - adults and children 12 years and older - • take 1 caplet every 4 to 6 hours while symptoms persist - • if ...

Other information
• read all warnings and directions before use - • store between 20-25°C (68-77°F) • avoid high humidity and excessive heat above 40°C (104°F) • see end panel for lot number and expiration date ...

•

read all warnings and directions before use

•

store between 20-25°C (68-77°F)

•

avoid high humidity and excessive heat above 40°C (104°F)

•

see end panel for lot number and expiration date

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Inactive ingredients
colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, iron oxides, microcrystalline cellulose, polyethylene glycol ...

colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, iron oxides, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, stearic acid, talc, titanium dioxide
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Questions?
Call 1-888-547-7400

Call 1-888-547-7400
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Principal Display Panel
see revised warning - Compare to active ingredient in Motrin® IB - ibuprofen tablets, 200 mg - pain reliever/fever reducer (NSAID) up & up™ 100 CAPLETS† (†CAPUSLE – SHAPED TABLETS) ACTUAL SIZE - 100 ...

see revised warning

Compare to active ingredient in Motrin® IB

ibuprofen tablets, 200 mg

pain reliever/fever reducer (NSAID)

up & up™

100 CAPLETS† (†CAPUSLE – SHAPED TABLETS)

ACTUAL SIZE

100 CAPLETS†

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INGREDIENTS AND APPEARANCE

Product Information

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adults and children 12 years and older	• take 1 caplet every 4 to 6 hours while symptoms persist • if pain or fever does not respond to 1 caplet, 2 caplets may be used • do not exceed 6 caplets in 24 hours, unless directed by a doctor
children under 12 years	• ask a doctor

Published Date (What is this?)	Version	Files
Sep 8, 2023	5 (current)	download
Dec 13, 2019	4	download
Jun 14, 2018	3	download
Dec 19, 2014	2	download
Oct 17, 2011	1	download

	RxCUI	RxNorm NAME	RxTTY
1	310965	ibuprofen 200 MG Oral Tablet	PSN
2	310965	ibuprofen 200 MG Oral Tablet	SCD
3	310965	ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet	SY

Label: UP AND UP IBUPROFEN- ibuprofen tablet, film coated

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Drug Label Info

Safety

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More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

Label: UP AND UP IBUPROFEN- ibuprofen tablet, film coated

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

UP AND UP IBUPROFEN- ibuprofen tablet, film coated

Number of versions: 5

UP AND UP IBUPROFEN- ibuprofen tablet, film coated

UP AND UP IBUPROFEN- ibuprofen tablet, film coated

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UP AND UP IBUPROFEN- ibuprofen tablet, film coated

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.