FDA label 263c8404-2706-9792-e063-6394a90ad2de

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
f7aa08fc-5d10-4067-8f20-3c3e176e3e35
SPL ID
263c8404-2706-9792-e063-6394a90ad2de
Version
3
Effective date
2024-11-06
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:49:24

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 ranitidine 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. ● with other acid reducers ● if you have kidney disease, except under the advice and supervision of a doctor ASK A DOCTOR BEFORE USE IF YOU HAVE o frequent chest pain o frequent wheezing, particularly with heartburn o unexplained weight loss o nausea or vomiting o stomach pain o had heartburn over 3 months. This may be a sign of a more serious condition. o heartburn with lightheadedness, sweating or dizziness o chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness Stop use and ask a doctor if o your heartburn continues or worsens o 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.