Label: MEDI-FIRST IBUPROFEN- ibuprofen tablet, coated
MEDI-FIRST PLUS IBUPROFEN- ibuprofen tablet, coated
MEDIQUE IPRIN- ibuprofen tablet, coated
DOVER ADDAPRIN- ibuprofen tablet, coated
OTIS CLAPP ULTRAPRIN- ibuprofen tablet, coated

  • NDC Code(s): 47682-700-13, 47682-700-47, 47682-700-64, 47682-700-69, view more
    47682-700-99, 47682-702-13, 47682-702-99, 47682-709-33, 47682-709-48, 47682-714-13, 47682-714-99, 47682-718-13, 47682-718-30, 47682-718-33, 47682-718-48, 47682-718-50, 47682-718-99
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 16, 2022

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Ibuprofen 200 mg (NSAID)

    *nonsteroidal antinflamatory drug

  • PURPOSE

    Purpose

    Pain reliever/fever reducer

  • INDICATIONS & USAGE

    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

    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

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

  • DO NOT USE

    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 DOCTOR

    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, kidney disease, asthma or had a stroke

    ■ you are taking a diuretic

  • ASK DOCTOR/PHARMACIST

    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

    When using this product

    ■ take with food or milk if stomach upset occurs

  • STOP USE

    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 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

  • PREGNANCY OR BREAST FEEDING

    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 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

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    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:

    Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    ■ read all product information before using

    ■ store at 68-77°F (20-25°C)

    ■ avoid excessive heat 104°F (above 40°C )

    ■ tamper evident sealed packets

    ■ do not use any opened or torn packets

  • INACTIVE INGREDIENT

    Inactive ingredients

    carnauba wax*, corn starch, hypromellose*, iron oxide red, lactose*, magnesium stearate*, microcrystalline cellulose*, polydextrose*, polyethylene glycol, polyvinyl alcohol*, povidone (K30)*, silicon dioxide, sodium starch glycolate, stearic acid, talc*, titanium dioxide

    *may contain

  • QUESTIONS

    Questions or comments? 1-800-634-7680

  • Medi-First Ibuprofen Label

    Medi-First®

    Ibuprofen 200 mg

    100 tablets (50 x 2)

    Pain Reliever/Fever Reducer

    Aches, Fever • Ibuprofen (NSAID) 200 mg

    Pull to Open

    Compare active ingredient to:

    Advil®

    Registered Trademark of Pfizer Consumer Healthcare

    This Package is for Households without Young Children.

    Tamper Evident Unit Dose Packets

    100R MF Ibuprofen

  • Medi-First Plus Ibuprofen Label

    Medi-First® Plus

    Ibuprofen

    Ibuprofen 200 mg (NSAID)

    100 Tablets (50 x 2’s)

    Pull To Open

    This Package isfor Households without Young Children.

    Pain Reliever/Fever Reducer

    Compare active ingredient to:

    Advil®

    Registered Trademark of Pfizer Consumer Healthcare

    Tamper Evident Unit Dose Packets

    100R MFP Ibuprofen

  • Medique Iprin Label

    Medique®

    I-Prin

    Ibuprofen 200 mg

    Anti-Inflammatory (NSAID)

    This Package is for Households without Young Children.

    Pull to Open

    Pain Reliever/Fever Reducer • Ibuprofen 200 mg

    200 Tablets (100 x 2)

    Tamper Evident Unit Dose Packets.

    100R IPrin

  • Dover Addaprin Label

    Dover Addaprin™

    Ibuprofen 200 mg Tablets (NSAID)

    Pain Reliever-Fever Reducer

    This Package is for Households Without Young Children.

    Dover Pharmaceutical

    Products of the highest quality and effectiveness

    Tamper Evident

    Sealed Packets

    Unit Dose Packs

    500 Tablets

    (250 Packets of 2)

    100R Dover Addaprin

  • Otis Clapp 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)

    Otis Clapp Ultraprin Label 1-31-19

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST IBUPROFEN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-718
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    TALC (UNII: 7SEV7J4R1U)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-718-13250 in 1 BOX01/26/2017
    1NDC:47682-718-992 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-718-48125 in 1 BOX01/26/2017
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-718-3350 in 1 BOX01/26/2017
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-718-304 in 1 BOX01/26/2017
    42 in 1 PACKET; Type 0: Not a Combination Product
    5NDC:47682-718-5025 in 1 BOX04/16/2019
    52 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/26/2017
    MEDI-FIRST PLUS IBUPROFEN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-709
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-709-48125 in 1 BOX01/26/2017
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-709-3350 in 1 BOX01/26/2017
    22 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/26/2017
    MEDIQUE IPRIN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-700
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POVIDONE K30 (UNII: U725QWY32X)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    TALC (UNII: 7SEV7J4R1U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-700-693 in 1 BOX01/26/2017
    1NDC:47682-700-992 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-700-6412 in 1 BOX01/26/2017
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-700-47100 in 1 BOX01/26/2017
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-700-13250 in 1 BOX01/26/2017
    42 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/26/2017
    DOVER ADDAPRIN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-714
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-714-13250 in 1 BOX01/26/2017
    1NDC:47682-714-992 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/26/2017
    OTIS CLAPP ULTRAPRIN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-702
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    TALC (UNII: 7SEV7J4R1U)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    POVIDONE K30 (UNII: U725QWY32X)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-702-13250 in 1 BOX02/01/201704/03/2017
    1NDC:47682-702-992 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917411/17/201404/03/2017
    Labeler - Unifirst First Aid Corporation (832947092)