FDA label f42adf39-8452-9387-e053-2995a90a06fb

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: 419f7095-706e-4dcd-a670-1ef772c08cc4
SPL ID: f42adf39-8452-9387-e053-2995a90a06fb
Version: 2
Effective date: 2023-02-08
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:58:13

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		f42adf39-8452-9387-e053-2995a90a06fb	id
spl set id		419f7095-706e-4dcd-a670-1ef772c08cc4	set_id

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. OTC - DO NOT USE SECTION • If you are sensitive to any ingredient in this product. OTC - WHEN USING SECTION • Remove contact lenses before using • To avoid contamination, do not touch tip of container to any surface • replace cap after using. OTC - STOP USE SECTION AND ASK A DOCTOR IF you feel eye pain, changes in vision occur, Redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours. Keep out of the reach of children. If swallowed, 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.