FDA label 1a3fbfb6-eb14-4854-bc5c-9fb1fcfbc12b

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
7d1af7eb-b73f-4980-a321-f8a04075df41
SPL ID
1a3fbfb6-eb14-4854-bc5c-9fb1fcfbc12b
Version
2
Effective date
2025-05-28
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:27:43

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 ▪ frequent chest pain ▪ frequent wheezing, particularly with heartburn ▪ unexplained weight loss ▪ nausea or vomiting ▪ stomach pain ▪ 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 Stop use and ask a doctor if ▪ your heartburn continues or worsens ▪ you need to take this product for more than 14 days 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).

Reported adverse events (FAERS/openFDA)#

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