Nasal Rinse Mix

Manufacturer
ZheJiang Longmed Medical Technology Co., Ltd.
Effective date
2024-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:58:59

Label at a glance#

ProductNasal Rinse Mix
Active ingredientSODIUM CHLORIDE
Label structure8 sections

Storage and handling

Inspect saline packets for integrity. Do not use saline packets if open, torn, orexpired. Protect saline packets from excessive heatand moisture. See saline packets or box for lot #t andexpiration date.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 100%

OTC - PURPOSE SECTION

Nasal wash

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Temporarily relieves symptoms associated withsinusitis, cold, flu or allergies:
Sneezing
Runny nose
Nasal stuffiness
Post nasal drip
Removes inhaled irritants (dust, pollen)
Promotes nasal and sinus drainage
Helps reduce swelling of nasal membranes
Moisturizes dry nasal passages

WARNINGS SECTION

Stop use and ask a doctor if washing isuncomfortable or symptoms are not relieved
Do not use unfiltered tap water, see instruc-tions inside box for proper water sources.
Do not use if nasal passages are completelyblocked or if you have an ear infection orblocked ears.
Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions
Adults and children 4 years and over: Use 1-2packets per 7 oz(200 ml) of water.Children under 4 years: Consult a physician

STORAGE AND HANDLING SECTION

Inspect saline packets for integrity.
Do not use saline packets if open, torn, orexpired.
Protect saline packets from excessive heatand moisture.
See saline packets or box for lot #t andexpiration date.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84534-001NASAL RINSE MIX (SODIUM CHLORIDE) GRANULE [ZHEJIANG LONGMED MEDICAL TECHNOLOGY CO., LTD.]1Unmatched20240716_1d43a1c7-66e8-1dc9-e063-6294a90aa1b5.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84534-00184534-001-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

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
397c04ed-6834-7fbf-e063-6294a90a66441d43a1c7-66e8-1dc9-e063-6294a90aa1b52025-07-09WarningsExact identifier
spl set id: 1d43a1c7-66e8-1dc9-e063-6294a90aa1b5

Reported adverse events (FAERS/openFDA)#

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