FDA label 612165d6-dc0b-464e-90fb-fbf63b1a749b

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
06d7a21c-c318-4f97-802b-1889401b6288
SPL ID
612165d6-dc0b-464e-90fb-fbf63b1a749b
Version
1
Effective date
2021-12-15
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:47

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 consume if there is anything wrong with product before ingestion. ■ If you have specific constitution or allergic, please check the ingredients before ingestion. ■ If a child swallows tablets, it can get caught in the throat, so care must be taken not to swallow them. ■ Infants, pregnant women, lactating women, disease holders, or those taking drugs should consult a doctor, pharmacist, etc. before ingestion. ■ Please be careful because you should not take the "dehumidifier" packaged separately for food quality control. ■ Consult with an expert in the case of an abnormal case.

Reported adverse events (FAERS/openFDA)#

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