Label: NAPROXEN SODIUM tablet, film coated
- NDC Code(s): 11822-6040-2, 11822-6040-5, 11822-6040-6, 11822-6040-7, view more
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 12, 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 caplet)
Naproxen sodium 220 mg (naproxen 200 mg) (NSAID)* *nonsteroidal anti-inflammatory drug
-
Purpose
Pain reliever/fever reducer
-
Uses
temporarily relieves minor aches and pains due to: headache - muscular aches - the common cold - toothache - menstrual cramps - backache - minor pain of arthritis - temporarily reduces fever
-
Warnings
Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: asthma (wheezing) skin reddening - shock - blisters - rash - facial ...
-
Directions
do not take more than directed - the smallest effective dose should be used - drink a full glass of water with each dose - adults and children 12 years and older - take 1 caplet every 8 to 12 hours ...
-
Other information
each caplet contains: sodium 20 mg - store at 20°-25°C (68°-77°F). Avoid high humidity and excessive heat above 40°C (104°F) see end flap for expiration date and lot number
-
Inactive ingredients
croscarmellose sodium, FD&C blue #2 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, silicon dioxide, talc, titanium dioxide
-
Questions or comments?
Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday
-
Principal display panel
NDC 11822-6040-6 - Compare to the - active ingredient of - Aleve® Caplets† STRENGTH TO LAST 12 HOURS - NAPROXEN - SODIUM - NAPROXEN SODIUM - TABLETS, 220 mg - PAIN RELIEVER/ FEVER ...
-
INGREDIENTS AND APPEARANCEProduct Information