Active Ingredient (In Each Capsule)
Lansoprazole 15 mg
The following Structured Product Label (SPL) was submitted to the FDA by Our Family (nash Finch Company) for the product Heartburn Relief 24 Hour (NDC 70253-019). 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, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are taking, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lansoprazole 15 mg
Acid reducer
Allergy alert: Do not use if you are allergic to lansoprazole
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
colloidal silicon dioxide, D & C Red No. 33, D & C Yellow No. 10, FD & C Blue No. 1, FD & C Red No. 40, gelatin, hypromellose, magnesium carbonate, methacrylic acid copolymer dispersion, polyethylene glycol, polysorbate 80, sucrose, sugar spheres, talc, titanium dioxide
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Compare to the active ingredient in Prevacid® 24 HR*
*Prevacid® 24 HR is a registered trademark of Takeda Pharmaceuticals North America, Inc., and is used under license. ©2012 Novartis Consumer Health. Inc
HEARTBURN RELIEF 24 HOUR™
Lansoprazole Delayed- Release capsules, 15 mg
ACID REDUCER
Sodium Free
Product of India
KEEP OUTER CARTON AND PACKAGE INSERT. THEY CONTAIN IMPORTANT INFORMATION.
TAMPER-EVIDENT BOTTLE: DO NOT USE IF INNER FOIL SEAL IMPRINTED WITH “SEALED for YOUR PROTECTION” OR DARK BLUE TO BLACK GELATIN BAND AROUND THE CENTER OF EACH CAPSULE IS MISSING OR BROKEN.
* Please review the disclaimer below.