Label: IBUPROFEN MINI capsule, liquid filled

  • NDC Code(s): 53345-050-01
  • Packager: Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 2, 2019

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  • Active ingredient (in each capsule)
    Solubilized ibuprofen equal to 200 mg ibuprofen (NSAID)** (present as the free acid and potassium salt) **nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever/Fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: headache - toothache - backache - menstrual cramps - 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: hives - facial swelling - asthma (wheezing) shock - skin ...
  • Directions
    do not take more than directed - the smallest effective dose should be used - adults and children 12 years and over: take 1 capsule every 4 to 6 hours while symptoms persist - if pain or fever does ...
  • Other information
    each capsule contains: potassium 20 mg - read all warnings and directions before use. store at 20°-25°C (68°-77°F) avoid excessive heat above 40°C (104°F)
  • Inactive ingredients
    FD&C green #3, gelatin, medium chain triglycerides, polyethylene glycol, potassium hydroxide, purified water, sorbitol sorbitan solution, and white ink
  • Questions or commonts
    Call toll free: 1-855-215-8180
  • Ibuprofen Capsules 200 mg Mini
    Each softgel contains: Ibuprofen 200 mg Mini - CAUTION: FOR FURTHER MANUFACTURING, PROCESSING OR REPACKAGING - Quantity: 12,000 Capsules - NDC No.:53345-050-01 - MADE IN CHINA - IMPORTANT: 1.Inspect ...
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    Product Information