FDA label dde8e58a-8b52-4404-8238-8c22a21c9daf

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
17861bc1-d560-49a7-90a9-cd978b708a0a
SPL ID
dde8e58a-8b52-4404-8238-8c22a21c9daf
Version
3
Effective date
2014-10-17
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:53

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. Do not use n near the mouth or eyes n with known sensitivities to any listed ingredients n on children under 2 years of age unless directed by a doctor When using this product avoid eye contact. If accidental eye contact occurs, rinse thoroughly with water for 10-15 minutes. Stop use and ask a doctor if rash or irritation occurs, or if no improvement is seen after four weeks. If pregnant/breast-feeding, consult a health professional before using. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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