FDA label a9d424e9-4891-4035-b3f7-86caffccbf0a

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
548f7902-37d3-47ae-94ae-5af1ba9f142a
SPL ID
a9d424e9-4891-4035-b3f7-86caffccbf0a
Version
3
Effective date
2014-10-20
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:10:43

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 For external use only . Do not use near the mouth or eyes with known sensitivities to any listed ingredients 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.