FDA label df50bade-c0e2-4958-9d19-1db4ddac7e4c

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
4726a62c-ea5c-427e-9900-8a828f5a8ddb
SPL ID
df50bade-c0e2-4958-9d19-1db4ddac7e4c
Version
2
Effective date
2014-11-20
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:06

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 lady's slipper or orchids you are lactose intolerant Stop use and ask a doctor if symptoms persist continuously for more than 2 weeks or worsen. Insomnia (sleeplessness) may be a symptom of serious underlying illness. If pregnant or breast feeding , ask a health professional before use. Keep this and all medicines out of reach of children.

Reported adverse events (FAERS/openFDA)#

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