Saline Wipes by Ningbo Riway Daily Commodity Co., Ltd

Saline Wipes by

Drug Labeling and Warnings

Saline Wipes by is a Otc medication manufactured, distributed, or labeled by Ningbo Riway Daily Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SALINE WIPES- sodium chloride cloth 
Ningbo Riway Daily Commodity Co., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Active Ingredient(s)

Sodium chloride .90%

Purpose

Nasal Decongestant

Use

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

Warnings

For external use only.

Do not use

If you are allergic to any of the ingredients.

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

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

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

Directions

Remove wipe and unfold.

Gently wipe the nose and face.

Throw used wipe in trash. Do not flush.

Inactive ingredients

Purified Water, Aloe Barbadensis Leaf Extract.

Package Label - Principal Display Panel

SALINE WIPES 
sodium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77267-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	0.9 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77267-007-01	259.2 mL in 1 BAG; Type 0: Not a Combination Product	10/17/2020	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/17/2020	12/31/2023

Labeler - Ningbo Riway Daily Commodity Co., Ltd (540997562)

Registrant - Ningbo Riway Daily Commodity Co., Ltd (540997562)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Riway Daily Commodity Co., Ltd		540997562	manufacture(77267-007)

Revised: 12/2025

Document Id: 47283929-fdf5-fefa-e063-6394a90a8d25

34390-5

Set id: b1d29407-6911-c023-e053-2995a90a6dcc

Version: 3

Effective Time: 20251230