Active Ingredient (In Each Capsule)
Lansoprazole USP, 15 mg
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Lansoprazole (NDC 11673-324). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each capsule), purpose, use, warnings, do not use if you have, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lansoprazole USP, 15 mg
Acid reducer
Allergy alert:
Symptoms may include:
If an allergic reaction occurs, stop use and seek medical help right away.
ask a healthcare professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
D&C Red 28, FD&C Blue No.1, FD&C Green 3, FD&C Red 40, gelatin, hydroxypropyl cellulose, iron oxide black, low substituted hydroxypropyl cellulose, magnesium carbonate, methacrylic acid copolymer, polyethylene glycol 6000, polysorbate 80, sodium lauryl sulphate, starch (corn), sucrose, sugar spheres, talc, titanium dioxide
call 1-888-375-3784
* Please review the disclaimer below.