FDA label d6947c1d-0df1-4207-e053-2995a90ad2d4

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
b946019a-1896-24b3-e053-2995a90a216f
SPL ID
d6947c1d-0df1-4207-e053-2995a90ad2d4
Version
2
Effective date
2022-01-27
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:42

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

Ask a Doctor before use if you are: experiencing worsening symptoms or if symptoms persist more than 7 days, have a diagnosed heart arrythmia, under 12 yrs. When using this product You may get drowsy avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowziness be careful when driving a motor vehicle or operating machinery If pregnant or breast-feeding, ask a health professional before use Keep out of reach of chldren. In case of overdose, get medical help or contact posion Control Center right away

Reported adverse events (FAERS/openFDA)#

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