FDA label b4df1e62-2587-fff7-e053-2a95a90aca06

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
3ba808e8-cac3-4d08-a8d2-3e3f6905373e
SPL ID
b4df1e62-2587-fff7-e053-2a95a90aca06
Version
3
Effective date
2020-11-24
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 05:40:43

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 use if you have an allergy or hypersensitivity to components of the formula or if you have had a prior reaction to this product. Ask a doctor before use if you are under a doctor's care for any serious condition taking any other drug When using this product do not exceed the recommended daily dosage unless directed by a physician Stop use and ask a doctor if symptoms persist, worsen, or if new symptoms occur after 7 days rash develops If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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