IBUPROFEN PM - diphenhydramine citrate and ibuprofen tablet, coated 
Walgreen Company

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Walgreen Co. Ibuprofen PM Drug Facts

Active ingredient (in each caplet)

Diphenhydramine citrate 38 mg

Ibuprofen 200 mg (NSAID)*

*nonsteroidal anti-inflammatory drug

Purpose

Nighttime sleep-aid

Pain reliever

Uses

Warnings

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

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

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,

ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of 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)

Directions

Other information

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, glyceryl behenate, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, talc, titanium dioxide

Questions or comments?

1-800-719-9260

Principal Display Panel

New!

Ibuprofen PM

Ibuprofen, 200mg/Diphenhydramine Citrate, 38mg Tablets

Pain Reliever (NSAID)/Nighttime Sleep-Aid

See New Warnings Information

(**Capsule-shaped tablets)

Caplets

Ibuprofen PM Carton Image #1

Ibuprofen PM Carton Image #1

Ibuprofen PM Carton Image #2

Ibuprofen PM Carton Image #2


IBUPROFEN  PM
diphenhydramine citrate, ibuprofen   tablet, coated
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)0363-0413
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE CITRATE (DIPHENHYDRAMINE) DIPHENHYDRAMINE CITRATE38 mg
IBUPROFEN (IBUPROFEN) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
COLLOIDAL SILICON DIOXIDE 
CROSCARMELLOSE SODIUM 
GLYCERYL BEHENATE 
HYDROXYPROPYL CELLULOSE 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOL 
POLYVINYL ALCOHOL 
TALC 
TITANIUM DIOXIDE 
Product Characteristics
ColorWHITEScore no score
ShapeCAPSULESize15mm
FlavorImprint Code L413
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
10363-0413-271 BOTTLE In 1 CARTONcontains a BOTTLE
180 TABLET In 1 BOTTLEThis package is contained within the CARTON (0363-0413-27)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07911302/09/2010

Labeler - Walgreen Company (008965063)
Revised: 02/2011Walgreen Company