0.9 percentsaline

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
0.9 percentsaline
Generic name
SODIUM CHLORIDE
Manufacturer
Huizhou Jinsheng Medical Technology Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
487cb4fc-2e0b-020f-e063-6294a90a4526
SPL ID
487cb4fc-2e0c-020f-e063-6294a90a4526
Version
1
Effective date
2026-02-03
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 05:48:58
Harmonized routes table
Harmonized routes
CUTANEOUS, NASAL, OPHTHALMIC, TOPICAL

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

NOT FOR INJECTION Only use sealed vials do not use if vial is broken or already open Do not use After expiration date Discontinue if you experience any adverse reaction and call your physician Not for injection, for extemal use only Do not use if allergicto any of stated Ingredients,if irritation occurs, discon tinue use and consult your doctor or speclalist Do not heat liqud Do not use after erplry date Do not use unless seals Intact before use

Reported adverse events (FAERS/openFDA)#

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