FDA.reportPublic FDA data

FDA label 8c1d1cab-b4ff-4937-b49c-5fcf1bd84044

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
f6cade29-479c-4eff-9973-ef8289ec0e36
SPL ID
8c1d1cab-b4ff-4937-b49c-5fcf1bd84044
Version
5
Effective date
2023-11-28
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 01:43:27

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 use if you are allergic to iodine Stop use and ask a doctor if you have a persistent or chronic cough such as occurs with, smoking, asthma, chronic bronchitis, or emphysema or if cough is accompanied by excessive phlegm (mucus). symptoms persist for more than 7 days, recur, or are accompanied by fever, rash, or headache. 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.

Reported adverse events (FAERS/openFDA)#

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