WET ONES ANTIBACTERIAL HAND WIPES OCEAN BREEZE- benzalkonium chloride swab

Wet Ones Antibacterial Hand Wipes Ocean Breeze by

Drug Labeling and Warnings

Wet Ones Antibacterial Hand Wipes Ocean Breeze by is a Otc medication manufactured, distributed, or labeled by Edgewell Personal Care Brands LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.11%

Purpose

Antibacterial

Use

to decrease bacteria on skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients.

if irritation and redness develop.

When using this product

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor

if condition persists for more than 72 hours.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 3 years and over: rub hands thoroughly with product and allow skin to dry without wiping

Children under 3 years: ask a doctor before use.

Inactive ingredients

Water, Ethyl Alcohol, Propylene Glycol, Phenoxyethanol, Lauryl Glucoside, Iodopropynyl Butylcarbamate, Tetrasodium EDTA, 2-Bromo-2-Nitropropane-1,3-DIol, Citric Acid, Fragrance, Aloe Barbadensis Leaf Extract, Chamomilla, Recutita (Matricaria) Flower Extract

Questions or Comments?

Call 1-866-WET-111S

(1-866-938-1117), M-F

Primary Display Panel

Wet

Ones(R)

ANTIBACTERIAL

HAND WIPES

Ocean Breeze

Touch of Aloe

Wet

Ones

ANTIBACTERIAL HAND WIPES

Ocean Breeze

Touch of Aloe

ANTIBACTERIAL

25

wipes

ANTIBACTERIAL

Soft Texture

50

wipes

INGREDIENTS AND APPEARANCE

WET ONES ANTIBACTERIAL HAND WIPES OCEAN BREEZE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-903
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.11

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BRONOPOL (UNII: 6PU1E16C9W)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-903-25	25 in 1 POUCH; Type 0: Not a Combination Product	01/08/2021
2	NDC: 63354-903-50	50 in 1 POUCH; Type 0: Not a Combination Product	01/08/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/08/2021

Labeler - Edgewell Personal Care Brands LLC (151179769)