Home FDA labels f449a142-9e8f-6240-e053-2995a90aeb5b FDA label f449a142-9e8f-6240-e053-2995a90aeb5b 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 d2356ca9-99e8-40eb-9976-940a69f8a83f
SPL ID f449a142-9e8f-6240-e053-2995a90aeb5b
Version 3
Effective date 2023-02-09
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 06:09:46 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 2 matching rows.
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 STOP USE AND ASK DOCTOR If symptoms persistor recur, discontinue use. If pregnant or nursing a baby, consult a licensed practitioner before using this product. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.