FDA.reportPublic FDA data

Saline Wound Wash

Manufacturer
Safeway, Inc. | WPS | BOV Solution Inc
Effective date
2020-12-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:00:41

Label at a glance#

ProductSaline Wound Wash
Active ingredientBENZETHONIUM CHLORIDE
Label structure5 sections

Dosage and administration

clean the affected area • spray a small amount of this product on the area 1 to 3 fimes a day • may be covered with a stenle bandage • if bandaged, let dry first

Label contents#

Full prescribing information#

Warnings For external use only

WARNINGS SECTION

Do not use • in the eyes or apply over large areas of the body • longer than 1 week, unless directed by a doctor
Ask a doctor before use if you have • deep or puncture wounds, animal bites or serious burns
When using this product • avoid spraying in eyes • contents under pressure.

Do not puncture or incinerate • do not store at temperatures above 120'F.
Stop use and consult a doctor if • condition persists or gets worse
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

clean the affected area
• spray a small amount of this product on the area 1 to 3 fimes a day
• may be covered with a stenle bandage
• if bandaged, let dry first

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract (Aloe Vera), Benzalkonium Chlonde, Maltodextnn, Purmed Water, Sodium Bicarbonate, Sodium Chloride.

Questions?

OTC - QUESTIONS SECTION

1-888-723-3929

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21130-10321130-103-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

Source Document#

Source XML · Source PDF

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
b6fbb8a7-d47c-2bb5-e053-2995a90a8e1e6d65b0ae-ac91-4faa-8461-001c605786fc2020-12-21WarningsExact identifier
spl id: b6fbb8a7-d47c-2bb5-e053-2995a90a8e1e
spl set id: 6d65b0ae-ac91-4faa-8461-001c605786fc

Reported adverse events (FAERS/openFDA)#

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