FDA label bb43c7e0-d9d0-11de-b59b-0002a5d5c51b

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
b504a8e0-d9d0-11de-8c2a-0002a5d5c51b
SPL ID
bb43c7e0-d9d0-11de-b59b-0002a5d5c51b
Version
1
Effective date
2009-11-30
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:04

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: Side effects may include headahce, nausea, sore throat, allergic rhinitis and gastointestinal upset. If symptoms persist or worsen, stop using this product and consult a physician. When using this product, avoid contact with the eyes. If product gets into the eyes, flush with water. Seek medical attention.

Reported adverse events (FAERS/openFDA)#

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