ACTIVE INGREDIENT

Manufacturer
Yiwu Huanshu E-commerce Co., Ltd
Effective date
2026-07-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-17 21:45:38

Label at a glance#

ProductWHWSWB 0.9% Saline
Active ingredientSODIUM CATION
Label structure11 sections

Indications and uses

For moisturizing dry nasal passages

Dosage and administration

Use as needed. Use with compatible nasal and respiratory care devices only as directed.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride USP 0.9%

Purpose

OTC - PURPOSE SECTION

Moisturizer

Uses

INDICATIONS & USAGE SECTION

For moisturizing dry nasal passages

Warnings

WARNINGS SECTION

· NOT FOR INJECTION

· Do not use if the ampoule is damaged or already open

· Do not use after expiration date

· Discontinue if you experience any adverse reaction and call your physician

· Keep out of reach of children

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Other information

OTHER SAFETY INFORMATION

· Store at room temperature 15° to 30°C (59° to 86°F). Avoid excessive heat and protect from freezing

· This product has no preservatives. After opening the ampoule use immediately and discard after use to avoid risk of contamination.

Questions or comments

PATIENT COUNSELING INFORMATION

whwswb@outlook.com

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Use as needed.
Use with compatible nasal and respiratory care devices only as directed.

RECENT MAJOR CHANGES SECTION

Highlights:
the heading(s) of the changed section(s): Indications and Usage
identifying number of the corresponding changed section : 4
​the date on which the change was incorporated in the labeling:7/2026

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3030

DailyMed Product Concepts#

Product concept, Relation, Version table
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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87561-00187561-001-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CATIONLYR4M0NH37ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-04-04full-release2026-06-01 01:53:53

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WHWSWB 0.9% SalineSODIUM CHLORIDEYiwu Huanshu E-commerce Co., Ltd4e9c21e5-f2f9-90e4-e063-6394a90acfe22026-07-11WarningsExact identifier
ndc (package): 87561-001-00
ndc (product): 87561-001
ndc11 (package): 87561000100
spl id: 565825ff-6d64-606b-e063-6294a90a56aa
spl set id: 4e9c21e5-f2f9-90e4-e063-6394a90acfe2

Reported adverse events (FAERS/openFDA)#

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