FDA label 0daae8b7-d995-4bdc-9a60-6b34ff233eb7

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: 4b60e9d5-8b77-48c6-b879-ea6e0e9b1700
SPL ID: 0daae8b7-d995-4bdc-9a60-6b34ff233eb7
Version: 1
Effective date: 2019-03-13
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:22:21

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		0daae8b7-d995-4bdc-9a60-6b34ff233eb7	id
spl set id		4b60e9d5-8b77-48c6-b879-ea6e0e9b1700	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.