Label: IBUPROFEN tablet, film coated
- NDC Code(s): 63981-291-03, 63981-291-14
- Packager: COSTCO WHOLESALE CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 16, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active ingredient (in each brown tablet)
Ibuprofen USP, 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug
-
Purpose
Pain reliever/fever reducer
-
Uses
temporarily relieves minor aches and pains due to: backache - menstrual cramps - toothache - headache - the common cold - muscular aches - minor pain of arthritis - temporarily reduces fever
-
Warnings
Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: facial swelling - shock - asthma (wheezing) skin ...
-
Directions
do not take more than directed - the smallest effective dose should be used - adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist - if pain or fever does ...
-
Other information
use by expiration date on package - store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F)
-
Inactive ingredients
carnauba wax, colloidal silicon dioxide, corn starch, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium ...
-
Questions or comments?
Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday
-
Principal Display Panel
KIRKLAND - Signature - COMPARE TO - ADVIL® active ingredient** NDC 63981-291-14 - ITM. / ART. 808082 - IBUPROFEN - Tablets USP, 200 mg - Pain Reliever/Fever Reducer (NSAID) Actual ...
-
INGREDIENTS AND APPEARANCEProduct Information