Label: IBUPROFEN tablet, film coated
- NDC Code(s): 71141-178-22, 71141-178-32
- Packager: Lidl US LLC
- 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: headache - backache - toothache - the common cold - muscular aches - menstrual cramps - 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: skin reddening - asthma (wheezing) rash - facial ...
-
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 ...
-
Other information
store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F) use by expiration date on package
-
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
†Compare to the active - ingredient in - Advil® Tablets - NDC 71141-178-22 - Actual Size - 100 - COATED - TABLETS - Ibuprofen - TABLETS USP, 200 mg - PAIN RELIEVER/FEVER REDUCER (NSAID) by LiDL® TAMPER ...
-
INGREDIENTS AND APPEARANCEProduct Information