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
55820ff9-7b4b-2bce-e063-6394a90a8b43
SPL ID
55820ff9-7b4c-2bce-e063-6394a90a8b43
Version
1
Effective date
2026-06-30
Source export date
2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:15:08
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.