FDA label 38f72774-7c52-b84f-e063-6394a90a8e64

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: f6e4af32-d567-2b02-e053-6394a90aa7a0
SPL ID: 38f72774-7c52-b84f-e063-6394a90a8e64
Version: 8
Effective date: 2025-07-02
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:43

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		38f72774-7c52-b84f-e063-6394a90a8e64	id
spl set id		f6e4af32-d567-2b02-e053-6394a90aa7a0	set_id

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 DO NOT TAKE MORE THAN 24 TABLETS FOR ADULTS UP TO 60 YEARS OF AGE (0R 12 TABLETS FOR ADULTS 60 YEARS OF AGE AND OLDER) IN A 24 HOUR PERIOD NOR USE MAXIMUM DOSAGE FOR MORE THAN 2 WEEKS, EXCEPT UNDER THE ADVICE AND SUPERVISION OF A PHYSICIAN. ASK A DOCTOR BEFORE USE IF YOU HAVE A SODIUM RESTRICTED DIET. ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE TAKING A PRESCRIPTION DRUG. ANTACIDS MAY INTERACT WITH CERTAIN PRESCRIPTION DRUGS. STOP USE AND ASK A DOCTOR IF SYMPTOMS LAST MORE THAN 2 WEEKS. 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.