Other
Drug Facts
Product Repackaged and Distributed
with permission of manufacturer by:
Select Corporation Carrollton, TX 75007
The following Structured Product Label (SPL) was submitted to the FDA by Select Corporation for the product Zantac 360 (NDC 52904-926). 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 other, active ingredient (in each tablet), purpose, uses, allergy alert, do not use, ask a doctor before use if you have, otc - ask doctor/pharmacist, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Product Repackaged and Distributed
with permission of manufacturer by:
Select Corporation Carrollton, TX 75007
Famotidine USP 20 mg
Acid reducer
Do not use if you are allergic to famotidine or other acid reducers
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
carnauba wax, corn starch, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, red iron oxide, sodium starch glycolate, talc, titanium dioxide, yellow iron oxide
call 1-800-633-1610 or visit www.zantacotc.com
* Please review the disclaimer below.