Fendall Pure Flow

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)

Brand name
Fendall Pure Flow
Generic name
PURIFIED WATER
Manufacturer
Honeywell Safety Products USA, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
afda6fc3-7615-b0be-e053-2995a90a6208
SPL ID
28eea87a-8088-19aa-e063-6394a90aad4a
Version
9
Effective date
2024-12-10
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:45:29
Harmonized routes table
Harmonized routes
OPHTHALMIC

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 if solution changes color or gets cloud in open wounds in or near eyes with contact lenses Stop use and ask a doctor if you have changes in vision eye pain continued redness or irritation of the eyes or if the condition worsens or persists Keep out of 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.