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

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, AHC Ltd. 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

Principal Display Panel

Wet

Ones

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

WET ONES ANTIBACTERIAL HAND WIPES OCEAN BREEZE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-906
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 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-906-25	25 g in 1 POUCH; Type 0: Not a Combination Product	07/26/2022	04/30/2023
2	NDC: 63354-906-50	50 g in 1 POUCH; Type 0: Not a Combination Product	07/26/2022	06/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/26/2022	06/30/2023

Labeler - Edgewell Personal Care Brands LLC (151179769)

Establishment
Name	Address	ID/FEI	Business Operations
AHC Ltd		413138557	manufacture(63354-906)

Revised: 10/2023

Document Id: 0762b94b-c605-cb1c-e063-6294a90a5df4

34390-5

Set id: e4bb3209-4393-46ed-e053-2995a90a8db1

Version: 2

Effective Time: 20231010