FDA label f1e51714-95cf-562e-e053-2995a90ac56e

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
d1ef5e04-4b55-b923-e053-2995a90a7264
SPL ID
f1e51714-95cf-562e-e053-2995a90ac56e
Version
2
Effective date
2023-01-10
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:09:29

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 Not for oral use. There is enough boron in this package to cause serious harm if ingested. Consult a health care practitioner if symptoms persist or worsen. Consult a health care practitioner prior to use if you have been diagnosed with estrogen-dependent cancer or if you have a kidney disorder

Reported adverse events (FAERS/openFDA)#

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