Unifirst First Aid Corporation
UNIFIRST FIRST AID PRODUCTS
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
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 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 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 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 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)
MEDIQUE I-PRIN
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-209 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
115
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-209-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-209-99 |
2 in 1 PACKET |
|
|
3 |
NDC:47682-209-99 |
2 in 1 PACKET |
|
|
4 |
NDC:47682-209-99 |
2 in 1 PACKET |
|
|
5 |
NDC:47682-209-69 |
3 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA091237 |
2012-06-25 |
|
|
Otis Clapp Ultraprin
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-502 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
44;352
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-502-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-502-13 |
250 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA075139 |
2008-12-30 |
|
|
MEDI-FIRST Ibuprofen
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-829 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
115
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-829-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-829-99 |
2 in 1 PACKET |
|
|
3 |
NDC:47682-829-99 |
2 in 1 PACKET |
|
|
4 |
NDC:47682-829-99 |
2 in 1 PACKET |
|
|
5 |
NDC:47682-829-30 |
4 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA091237 |
2012-06-25 |
|
|
MEDI-FIRST PLUS Ibuprofen
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-929 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
115
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
|
2 in 1 PACKET |
|
|
2 |
|
2 in 1 PACKET |
|
|
3 |
NDC:47682-929-33 |
50 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA091237 |
2012-06-25 |
|
|
Dover Addaprin
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-309 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
115
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-309-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-309-13 |
250 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA091237 |
2012-06-25 |
|
|
Otis Clapp Ultraprin
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-409 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
115
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-409-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-409-13 |
250 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA091237 |
2012-06-25 |
|
|
MEDIQUE I-PRIN
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-100 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
44;352
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-100-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-100-99 |
2 in 1 PACKET |
|
|
3 |
NDC:47682-100-99 |
2 in 1 PACKET |
|
|
4 |
NDC:47682-100-99 |
2 in 1 PACKET |
|
|
5 |
NDC:47682-100-69 |
3 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA075139 |
2008-12-30 |
|
|
MEDI-FIRST Ibuprofen
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-808 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
44;352
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-808-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-808-99 |
2 in 1 PACKET |
|
|
3 |
NDC:47682-808-99 |
2 in 1 PACKET |
|
|
4 |
NDC:47682-808-99 |
2 in 1 PACKET |
|
|
5 |
NDC:47682-808-30 |
4 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA075139 |
2008-12-30 |
|
|
MEDI-FIRST PLUS Ibuprofen
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-908 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
44;352
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
|
2 in 1 PACKET |
|
|
2 |
|
2 in 1 PACKET |
|
|
3 |
NDC:47682-908-33 |
50 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA075139 |
2008-12-30 |
|
|
Dover Addaprin
Ibuprofen TABLET, FILM COATED
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:47682-314 |
Route of Administration
|
ORAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
Ingredient Name
|
Basis of Strength
|
Strength
|
IBUPROFEN IBUPROFEN |
|
200 mg
|
Product Characteristics
|
Color
|
Size
|
Imprint Code
|
Shape
|
white (white) |
10 mm |
44;352
|
ROUND |
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:47682-314-99 |
2 in 1 PACKET |
|
|
2 |
NDC:47682-314-13 |
250 in 1 BOX, UNIT-DOSE |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
ANDA |
ANDA075139 |
2008-12-30 |
|
|