FDA label 1a71c9ed-7a20-41e1-83f3-9fe1e7b104a1

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
f6fc940b-8fed-4f50-9ab1-8d07e1f77730
SPL ID
1a71c9ed-7a20-41e1-83f3-9fe1e7b104a1
Version
2
Effective date
2021-12-13
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:38:06

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: For external use only. If pregnant or breast-feeding, taking birth control or on hormone replacement therapy, ​ ask a health professional before use. ​Keep out of reach of children. ​ If swallowed, get medical help or contact a Poison Control Center right away. ​When using this product ​ - Do not get into eyes. ​Stop use and ask doctor if ​ - Condition worsens - symptoms last more than 7 days. This product is not intended as an alternative hormone therapy.

Reported adverse events (FAERS/openFDA)#

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