RESP EASE

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
RESP EASE
Generic name
SODIUM CHLORIDE
Manufacturer
Venture Healthcare Ltd
Product type
HUMAN OTC DRUG
SPL set ID
31b812c9-fb0a-5ee0-e063-6294a90a03e1
SPL ID
4d276e36-bfb9-a84d-e063-6394a90a9d9e
Version
2
Effective date
2026-03-16
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:31
Harmonized routes table
Harmonized routes
NASAL

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 NOT FOR INJECTION Only use sealed vials do not use if vial is broken or already open Keep out of reach of children Do not use after expiration date If you experience any adverse reaction discontinue use and call your physician • Keep out of reach of children • Do not use after expiration date Discontinue if you experience any adverse reaction and call your physician

Reported adverse events (FAERS/openFDA)#

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