Wet Ones Antibacterial Hand Wipes Ocean Breeze by Edgewell Personal Care Brands LLC

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]

WET ONES ANTIBACTERIAL HAND WIPES OCEAN BREEZE- benzalkonium chloride swab 
Edgewell Personal Care Brands LLC

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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

Remove Label

Wet

Ones

ANTIBACTERIAL HAND WIPES

Ocean Breeze

Touch of Aloe

Top Label 1

ANTIBACTERIAL

25

wipes

63354-903-25

ANTIBACTERIAL

Soft Texture

50

wipes

63354-903-50

WET ONES ANTIBACTERIAL HAND WIPES OCEAN BREEZE 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 63354-903
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.11 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
BRONOPOL (UNII: 6PU1E16C9W)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
CHAMOMILE (UNII: FGL3685T2X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
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)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 63354-903-2525 mL in 1 POUCH; Type 0: Not a Combination Product01/08/202107/31/2022
2NDC: 63354-903-5050 mL in 1 POUCH; Type 0: Not a Combination Product01/08/202107/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/08/202107/31/2022
Labeler - Edgewell Personal Care Brands LLC (151179769)

Revised: 10/2024