FDA label 0ad58b28-5a19-44b3-9e4e-e42843482f8f

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
dbdbf383-14f3-43de-bfe8-9f7eb62435c4
SPL ID
0ad58b28-5a19-44b3-9e4e-e42843482f8f
Version
1
Effective date
2019-03-13
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 05:16:47

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 Warnings ■ Pregnant of lactating women or who takes other medicines need to consult a professional before taking this product. ■ Idiosyncratic or allergic person need to decide to take this product after consulting a doctor ■ In case of abnormal symptom, stop taking this product and consult a medical doctor or inquire to customer service. ■ Make sure to check expiry date, and please follow suggested use instruction. ■ Avoid direct ray of light and keep in cool and dry place, and keep out of the child's reach. ■ Consume this product as soon as opening, owing to the possibility of moisture absorption.

Reported adverse events (FAERS/openFDA)#

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