FDA label 26d964f1-b9a8-8ecb-e063-6394a90ad73f

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
dd45b1fe-76f1-4486-9ec9-ad409208afb4
SPL ID
26d964f1-b9a8-8ecb-e063-6394a90ad73f
Version
5
Effective date
2024-11-14
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:41:05

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Allergy alert : Do not use if you are allergic to famotidine or other acid reducers DO NOT USE ● if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor. ● if you have kidney disease, except under the advice and supervision of a doctor ● with other acid reducers ASK A DOCTOR BEFORE USE IF YOU HAVE ● had heartburn over 3 months. This may be a sign of a more serious condition. ● heartburn with lightheadedness, sweating or dizziness ● chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness ● frequent chest pain ● frequent wheezing, particularly with heartburn ● unexplained weight loss ● nausea or vomiting ● stomach pain Stop use and ask a doctor if ● your heartburn continues or worsens ● you need to take this product for more than 14 days PREGNANCY OR BREAST FEEDING If pregnant or breast-feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.