FDA label 814234c4-4523-4bcc-9f31-94d785ca09bb

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
ac99f344-f0a7-4502-a06f-888a1b382edd
SPL ID
814234c4-4523-4bcc-9f31-94d785ca09bb
Version
9
Effective date
2018-10-09
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:27

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings and cautions

Hyperkalemia warning: Use of this product may cause hyperkalemia, a serious condition that must be treated promptly because it can affect cell function and proper heart function. This can occur even if you have used this product before. Stop use and seek immediate medical attention if the patient develops: muscle fatigue weakness abnormal heart beat (arrhythnmias) paralysis nausea [Complete Instructions Back Page] Caution: Federal law restricts this device to sale by or on the order of a licensed professional. Disclaimer: CAO Group believes this information to be accurate and is offered only for the benefit of its customers for use of the product under proscribed conditions. This document is not to be considered a warranty or guarantee of product performance, and CAO Group is not legally bound to such claims based on this document. Manufactured by CAO (China) Medical Equipment Co,. Ltd. for CAO Group, Inc. P 877.236.4408 F 801.256.9287 4628 West Skyhawk Drive, West Jordan, UT 84084-4501 U.S.A. www.caogroup.com 13 Sept 2010 SAL-CAI010 REV 06.18.01 20JUN2018

Reported adverse events (FAERS/openFDA)#

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