MEDIQUE I-PRIN - ibuprofen tablet, film coated
OTIS CLAPP ULTRAPRIN - 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
Unifirst First Aid Corporation

----------

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	Item Code (Source)	NDC:47682-209
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
POLYVINYL ALCOHOL
SILICON DIOXIDE
STARCH, CORN
TALC
TITANIUM DIOXIDE

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	115
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-209-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-209-99)
1	NDC:47682-209-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-209-13)
2	NDC:47682-209-47	100 PACKET (100 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-209-99)
2	NDC:47682-209-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-209-47)
3	NDC:47682-209-64	12 PACKET (12 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-209-99)
3	NDC:47682-209-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-209-64)
4	NDC:47682-209-69	3 PACKET (3 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-209-99)
4	NDC:47682-209-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-209-69)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091237	06/25/2012

OTIS CLAPP ULTRAPRIN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-502
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSES
LACTOSE
MAGNESIUM STEARATE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
POVIDONE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
STEARIC ACID
TITANIUM DIOXIDE
TRIACETIN

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	44;352
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-502-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-502-99)
1	NDC:47682-502-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-502-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075139	12/30/2008

MEDI-FIRST IBUPROFEN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-829
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
POLYVINYL ALCOHOL
SILICON DIOXIDE
STARCH, CORN
TALC
TITANIUM DIOXIDE

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	115
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-829-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-829-99)
1	NDC:47682-829-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-829-13)
2	NDC:47682-829-48	125 PACKET (125 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-829-99)
2	NDC:47682-829-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-829-48)
3	NDC:47682-829-33	50 PACKET (50 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-829-99)
3	NDC:47682-829-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-829-33)
4	NDC:47682-829-30	4 PACKET (4 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-829-99)
4	NDC:47682-829-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-829-30)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091237	06/25/2012

MEDI-FIRST PLUS IBUPROFEN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-929
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
POLYVINYL ALCOHOL
SILICON DIOXIDE
STARCH, CORN
TALC
TITANIUM DIOXIDE

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	115
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-929-48	125 PACKET (125 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET
1		2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-929-48)
2	NDC:47682-929-33	50 PACKET (50 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET
2		2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-929-33)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091237	06/25/2012

DOVER ADDAPRIN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-309
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
POLYVINYL ALCOHOL
SILICON DIOXIDE
STARCH, CORN
TALC
TITANIUM DIOXIDE

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	115
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-309-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-309-99)
1	NDC:47682-309-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-309-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091237	06/25/2012

OTIS CLAPP ULTRAPRIN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-409
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOLS
POLYVINYL ALCOHOL
SILICON DIOXIDE
STARCH, CORN
TALC
TITANIUM DIOXIDE

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	115
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-409-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-409-99)
1	NDC:47682-409-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-409-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA091237	06/25/2012

MEDIQUE I-PRIN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-100
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSES
LACTOSE
MAGNESIUM STEARATE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
POVIDONE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
STEARIC ACID
TITANIUM DIOXIDE
TRIACETIN

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	44;352
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-100-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-100-99)
1	NDC:47682-100-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-100-13)
2	NDC:47682-100-47	100 PACKET (100 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-100-99)
2	NDC:47682-100-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-100-47)
3	NDC:47682-100-64	12 PACKET (12 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-100-99)
3	NDC:47682-100-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-100-64)
4	NDC:47682-100-69	3 PACKET (3 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-100-99)
4	NDC:47682-100-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-100-69)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075139	12/30/2008

MEDI-FIRST IBUPROFEN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-808
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSES
LACTOSE
MAGNESIUM STEARATE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
POVIDONE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
STEARIC ACID
TITANIUM DIOXIDE
TRIACETIN

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	44;352
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-808-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-808-99)
1	NDC:47682-808-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-808-13)
2	NDC:47682-808-48	125 PACKET (125 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-808-99)
2	NDC:47682-808-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-808-48)
3	NDC:47682-808-33	50 PACKET (50 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-808-99)
3	NDC:47682-808-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-808-33)
4	NDC:47682-808-30	4 PACKET (4 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-808-99)
4	NDC:47682-808-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-808-30)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075139	12/30/2008

MEDI-FIRST PLUS IBUPROFEN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-908
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSES
LACTOSE
MAGNESIUM STEARATE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
POVIDONE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
STEARIC ACID
TITANIUM DIOXIDE
TRIACETIN

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	44;352
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-908-48	125 PACKET (125 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET
1		2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-908-48)
2	NDC:47682-908-33	50 PACKET (50 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET
2		2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-908-33)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075139	12/30/2008

DOVER ADDAPRIN
ibuprofen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-314
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ibuprofen (Ibuprofen)	Ibuprofen	200 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE
HYPROMELLOSES
LACTOSE
MAGNESIUM STEARATE
POLYDEXTROSE
POLYETHYLENE GLYCOLS
POVIDONE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
STARCH, CORN
STEARIC ACID
TITANIUM DIOXIDE
TRIACETIN

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	44;352
Contains

Packaging
#	Item Code	Package Description	Multilevel Packaging
1	NDC:47682-314-13	250 PACKET (250 PACKET) in 1 BOX, UNIT-DOSE	contains a PACKET (47682-314-99)
1	NDC:47682-314-99	2 TABLET, FILM COATED (2 TABLET) in 1 PACKET	This package is contained within the BOX, UNIT-DOSE (47682-314-13)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075139	12/30/2008

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 09/2012 Unifirst First Aid Corporation