FDA.reportPublic FDA data

FDA label 836f90e1-279a-4da4-b2cc-eb58fafefb60

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
f046edd8-54a0-4398-b513-96d08b0cbe85
SPL ID
836f90e1-279a-4da4-b2cc-eb58fafefb60
Version
3
Effective date
2017-03-01
Source export date
2026-08-17
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/2026-08-17/02a497ed455224db2b03c6e57c80c30915819e1b465153908a5d9e68e3a47b21/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 08:09:48

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 If you are pregnant or breast feeding, ask a healthcare provider before use. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to Berberis-Homaccord or any of its ingedients exists.