SALINE WOUND WASH- benzethonium chloride 0.13% spray

Saline Wound Wash by

Drug Labeling and Warnings

Saline Wound Wash by is a Otc medication manufactured, distributed, or labeled by Safeway, Inc., WPS, BOV Solution Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Benzethonium Chloride 0.13% .............................. .First Aid Antiseptic

PURPOSE

First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

Warnings For external use only

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.

KEEP OUT OF REACH OF CHILDREN

Directions

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

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

Questions?

1-888-723-3929

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SALINE WOUND WASH 
benzethonium chloride 0.13% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21130-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21130-103-05	201 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/29/2020

Labeler - Safeway, Inc. (009137209)

Registrant - WPS (117357136)

Establishment
Name	Address	ID/FEI	Business Operations
BOV Solution Inc		800463486	manufacture(21130-103)