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: 2026-10-30
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/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:31:58

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.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		0ad58b28-5a19-44b3-9e4e-e42843482f8f	id
spl set id		dbdbf383-14f3-43de-bfe8-9f7eb62435c4	set_id

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.