NebuClear MD Saline

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
NebuClear MD Saline
Generic name
NEBUCLEAR MD SALINE
Manufacturer
Blue Echo Care LLC
Product type
HUMAN OTC DRUG
SPL set ID
55806cb8-cf92-c4e5-e063-6394a90aaa2d
SPL ID
55823bd7-f261-45c5-e063-6394a90ae158
Version
2
Effective date
2026-06-30
Source export date
2026-10-12
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:12:30
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 Do not use after expiration date Discontinue if you experience any adverse reactions and call your physician Only use sealed vials Do not use if vial is broken

Reported adverse events (FAERS/openFDA)#

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