IBUPROFEN- ibuprofen capsule, coated 
H E B

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HEB 44-292

Active ingredient (in each brown caplet)

 Ibuprofen USP, 200 mg (NSAID)*
*nonsteroidal anti-inflammatory drug

Purpose

 Pain reliever/fever reducer

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

  • right before or after heart surgery
  • if you have ever had an allergic reaction to any other pain reliever/fever reducer 

Ask a doctor before use if

  • 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 problems or serious side effects from taking pain relievers or fever reducers

Ask a doctor or pharmacist before use if you are

  • under a doctor's care for any serious condition
  • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
  • 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 for longer than directed 

Stop use and ask a doctor if

  •  you experience any of the following signs of stomach bleeding:
    • feel faint
    • have bloody or black stools
    • vomit blood
    • have stomach pain that does not get better
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present in the painful area
  • any new symptoms appear

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 complication during delivery.

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

carnauba wax, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, microcrystallin cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium stach glycolate, stearic acid, titanium dioxide.

Questions or comments?

Call 1-800-426-9392
8:30 AM-4:00 PM ET, Monday - Friday

Principal Display Panel

Compare to the active ingredient in Advil® Caplets†

NDC 37808-922-13

H-E-B®

IBUPROFEN
Tablets USP, 200 mg

Pain Reliever/Fever Reducer (NSAID)

250 Coated Caplets**
**Capsule-shaped tablets 

Contains No Gluten

†This product is not manufactured or distributed by Pfizer Consumer Healthcare, owner of the registered trademark Advil® Caplets.
50844    ORG041129213

MADE WITH PRIDE AND CARE FOR H-E-B, SAN ANTONIO, TX 78204

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

HEB 44-292

HEB 44-292

IBUPROFEN 
ibuprofen capsule, coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-922
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg
Inactive Ingredients
Ingredient Name Strength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Color BROWN Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code 44;292
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37808-922-13 1 in 1 CARTON
1 250 in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075010 05/24/1988
Labeler - H E B (007924756)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(37808-922)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(37808-922)

Revised: 2/2013
Document Id: a87c9a68-91a0-4bbd-ad55-909e8288c727
Set id: 06173bcd-1e17-4bf8-95e6-d03593585446
Version: 1
Effective Time: 20130225
 
H E B