0.9saline

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
0.9saline
Generic name
SODIUM CHLORIDE
Manufacturer
Huizhou Jinsheng Medical Technology Co., Ltd
Product type
HUMAN OTC DRUG
SPL set ID
49e76aca-ca2b-3b95-e063-6394a90a875e
SPL ID
49e76987-6106-89fc-e063-6394a90a4ce0
Version
1
Effective date
2026-02-03
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:51
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

Consult your doctor or pharmacist before use if you have 1. If you have allergies, redness and other symptoms 2. Do not use if allergic to any of stated Ingredients,if irritation occurs, discontinue use and consult your doctor or specialist please use caution when using this product: 1. Do not use if the bottle is cracked 2. Do not use if there is a foreign body inside 3. For external use only NOT FOR INJECTION

Reported adverse events (FAERS/openFDA)#

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