Your browser does not support JavaScript! MEDIQUE I-PRIN (IBUPROFEN) TABLET, FILM COATED MEDI-FIRST IBUPROFEN (IBUPROFEN) TABLET, FILM COATED MEDI-FIRST PLUS IBUPROFEN (IBUPROFEN) TABLET, FILM COATED DOVER ADDAPRIN (IBUPROFEN) TABLET, FILM COATED OTIS CLAPP ULTRAPRIN (IBUPROFEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]
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RxNorm Names

MEDIQUE I-PRIN (ibuprofen) tablet, film coated
MEDI-FIRST IBUPROFEN (ibuprofen) tablet, film coated
MEDI-FIRST PLUS IBUPROFEN (ibuprofen) tablet, film coated
DOVER ADDAPRIN (ibuprofen) tablet, film coated
OTIS CLAPP ULTRAPRIN (ibuprofen) tablet, film coated
[Unifirst First Aid Corporation]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL Abbreviated New Drug Application
Drug Label Sections

Drug Facts

Active ingredient (in each tablet)

Ibuprofen 200 mg (NSAID*)

*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

Uses

Temporarily relieves minor aches and pains associated with

  • headache
  • toothache
  • backache
  • menstrual cramps
  • common cold
  • muscular aches
  • minor arthritis pain

Temporarily reduces fever.

Warnings

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

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

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

  • you have problems or serious side effects from taking pain relievers or fever reducers
  • 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, or kidney disease
  • you have asthma
  • 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
  • the risk of heart attack or stroke may increase if you use more than directed or 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 lasts for more than 10 days
  • fever gets worse or lasts for more than 3 days
  • redness or swelling is present in the painful area
  • any new or unexpected symptoms occur

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 specifically 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.

Directions

  • do not use more than directed
  • the smallest effective dose should be used
  • do not take longer than 10 days, unless directed by a doctor (see Warnings)

Adults and children: (12 years and older)

Take 1 tablet every 4 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:

Do not give to children under 12 years of age.

Other information

  • read all product information before using
  • store at 68-77°F (20-25°C)
  • avoid excessive heat 40°C (above 104°F)
  • tamper evident sealed packets
  • do not use any opened or torn packets

Inactive ingredients

carnauba wax*, cellulose*, colloidal silicon dioxide*, corn starch*, croscarmellose sodium*, hypromellose*, iron oxide red*, lactose*, magnesium stearate, microcrystalline cellulose, polydextrose*, polyethylene glycol, polyvinyl alcohol*, povidone*, pregelatinized starch*, silica*, sodium lauryl sulfate*, sodium starch glycolate*, stearic acid*, talc*, titanium dioxide, triacetate*, triacetin*

*may contain

Questions or comments? 1-800-634-7680

100R Medique Iprin Label

Collect MediBucks

See inside flap for more details

Medique® I-Prin

Ibuprofen 200 mg

Pain Reliever/Fever Reducer (NSAID)

Alivia el Dolor/Reduce la Fiebre (AINE)

Easy To Swallow Film Coated Tablets

Facil de Tragar Tabletas con Cubierta Pelicular

Pull to Open

Tire Para Abrir

500 Tablets (250 x 2)

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

100R Medique Iprin Label

100R MF Ibuprofen Label

100 tablets (50 x 2)

Medi-First®

Ibuprofen 200 mg

Pain Reliever/Fever Reducer (NSAID)

Pull to Open

Easy To Swallow Film Coated Tablets

Compare active ingredient to: Genuine Advil®

Registered Trademark of Pfizer Consumer Healthcare

Tamper Evident Unit Dose Packets

100R MF Ibuprofen Label

100R MFP Ibuprofen Label

100 tablets (50 x 2's)

Medi-First® Plus

Ibuprofen 200 mg USP

Pain Reliever/Fever Reducer (NSAID)

Easy To Swallow Film Coated Tablets

Compare active ingredient to:

Advil®

Registered Trademark of Pfizer Consumer Healthcare

Tamper Evident Unit Dose Packets

100R MFP Ibuprofen Label

100R Dover Addaprin Label

Dover Addaprin™

Pain Reliever-Fever Reducer

Ibuprofen 200 MG. Tablets (NSAID)

Dover Pharmaceutical

Products of the highest quality and effectiveness

Tamper Resistant

Sealed Packets

Unit Dose Packs

500 Tablets

(250 Packets of 2)

100R Dover Addaprin Label

100R OC Ultraprin Label

OC Otis Clapp

Quality & Integrity Since 1840

Ultraprin ™

Pain Reliever-Fever Reducer (NSAID)

Ibuprofen Tablets USP 200 mg

For Deep Seated Pain

See Warnings and Directions on Side Panel

Tear Out Along Perforation To Dispense

Professional Healthcare

500 Tablets (250 Packets of 2)

100R OC Ultraprin Label
MEDIQUE I-PRIN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:47682-076
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ibuprofen (Ibuprofen) Ibuprofen200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CELLULOSE, MICROCRYSTALLINE 
FERRIC OXIDE RED 
HYPROMELLOSES 
LACTOSE 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOLS 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
Colorbrown (brown) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code IP;140
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-076-13250 in 1 BOX, UNIT-DOSE
1NDC:47682-076-992 in 1 PACKET
2NDC:47682-076-47100 in 1 BOX, UNIT-DOSE
2NDC:47682-076-992 in 1 PACKET
3NDC:47682-076-6412 in 1 BOX, UNIT-DOSE
3NDC:47682-076-992 in 1 PACKET
4NDC:47682-076-693 in 1 BOX, UNIT-DOSE
4NDC:47682-076-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07133312/30/2008
MEDI-FIRST IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:47682-077
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ibuprofen (Ibuprofen) Ibuprofen200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CELLULOSE, MICROCRYSTALLINE 
FERRIC OXIDE RED 
HYPROMELLOSES 
LACTOSE 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOLS 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
Colorbrown (brown) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code IP;140
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-077-13250 in 1 BOX, UNIT-DOSE
1NDC:47682-077-992 in 1 PACKET
2NDC:47682-077-48125 in 1 BOX, UNIT-DOSE
2NDC:47682-077-992 in 1 PACKET
3NDC:47682-077-3350 in 1 BOX, UNIT-DOSE
3NDC:47682-077-992 in 1 PACKET
4NDC:47682-077-304 in 1 BOX, UNIT-DOSE
4NDC:47682-077-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07133312/30/2008
MEDI-FIRST PLUS IBUPROFEN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:47682-078
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ibuprofen (Ibuprofen) Ibuprofen200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CELLULOSE, MICROCRYSTALLINE 
FERRIC OXIDE RED 
HYPROMELLOSES 
LACTOSE 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOLS 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
Colorbrown (brown) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code IP;140
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-078-48125 in 1 BOX, UNIT-DOSE
12 in 1 PACKET
2NDC:47682-078-3350 in 1 BOX, UNIT-DOSE
22 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07133312/30/2008
DOVER ADDAPRIN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:47682-079
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ibuprofen (Ibuprofen) Ibuprofen200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CELLULOSE, MICROCRYSTALLINE 
FERRIC OXIDE RED 
HYPROMELLOSES 
LACTOSE 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOLS 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
Colorbrown (brown) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code IP;140
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-079-13250 in 1 BOX, UNIT-DOSE
1NDC:47682-079-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07133312/30/2008
OTIS CLAPP ULTRAPRIN 
ibuprofen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:47682-080
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Ibuprofen (Ibuprofen) Ibuprofen200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CELLULOSE, MICROCRYSTALLINE 
FERRIC OXIDE RED 
HYPROMELLOSES 
LACTOSE 
MAGNESIUM STEARATE 
POLYDEXTROSE 
POLYETHYLENE GLYCOLS 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
STARCH, CORN 
TITANIUM DIOXIDE 
Product Characteristics
Colorbrown (brown) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code IP;140
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-080-13250 in 1 BOX, UNIT-DOSE
1NDC:47682-080-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07133312/30/2008
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 9/2012
 
Unifirst First Aid Corporation

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