FDA label d43cda90-2dd6-d377-e053-2995a90aa7b0

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
56550bdc-b600-5b16-e054-00144ff8d46c
SPL ID
d43cda90-2dd6-d377-e053-2995a90aa7b0
Version
2
Effective date
2021-12-28
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:39

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

Ask a doctor before use if: pregnant or nursing a baby, under 3 years of age If symptons persist for more than two days or worsen, contact a licensed health care professional. Do not use if imprinted tamper band is broken or missing. In case of accidental overdose, contact a Poison Control Center immediately. In case of emergency, the manufacturer may be contacted 24 hours a day, 7 days a week at (800) 624-9659.

Reported adverse events (FAERS/openFDA)#

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