FDA.reportPublic FDA data

Saline Wipes

Manufacturer
Ningbo Riway Industrial Co., Ltd.
Effective date
2023-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:20:19

Label at a glance#

ProductSaline Wipes
Active ingredientSODIUM CHLORIDE
Label structure12 sections

Dosage and administration

Remove wipe and unfold. Gently wipe the nose and face. Throw used wipe in trash. Do not flush.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium chloride .90%

Purpose

OTC - PURPOSE SECTION

Nasal Decongestant

Use

INDICATIONS & USAGE SECTION

For nasal decongestant and gentle cleansing of the nose and facial areas.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

When using this product,avoid contact with eyes and mouth. If product gets in the eyes,flush thoroughly with water.

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove wipe and unfold.

Gently wipe the nose and face.

Throw used wipe in trash. Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Barbadensis Leaf Extract.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SALINE WIPES PACKAGING FINAL 3SALINE WIPES PACKAGING FINAL 3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77267-007SALINE WIPES (SODIUM CHLORIDE) CLOTH [NINGBO RIWAY INDUSTRIAL CO., LTD.]2Legacy NDC20231122_b1d29407-6911-c023-e053-2995a90a6dcc.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77267-00777267-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLUCONOLACTONEWQ29KQ9POTIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM CHLORIDE451W47IQ8XACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
47283929-fdf5-fefa-e063-6394a90a8d25b1d29407-6911-c023-e053-2995a90a6dcc2025-12-30WarningsExact identifier
spl set id: b1d29407-6911-c023-e053-2995a90a6dcc

Reported adverse events (FAERS/openFDA)#

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