WET ONES- benzalkonium chloride swab

WET ONES by

Drug Labeling and Warnings

WET ONES 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 0.13%

Purpose

Antimicrobial Agent

Use

decreases bacteria on skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients.

When using this product

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues 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 2 years and over: Rub on hands for 30 seconds and allow skin to dry without wiping.

children under 2 years: ask a doctor before use.

Inactive Ingredients

Water, Alcohol Denat., Phenoxyethanol, PEG-8 Dimethicone, Caprylyl Glycol, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Potassium Sorbate, Fragrance, Disodium EDTA, Citric Acid, Aloe Barbadensis Leaf Juice.

Questions or Comments?

Call 1-866-WET-111S (1-866-938-1117), M-F

Principal Display Panel

TEAR HERE
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Lavender Scent
KILLS 99.99% OF GERMS*
8 Hour Moisturization
*Effective at killing 99.99%
of many common harmful
bacteria in as little as
15 seconds
1 WIPE

TEAR HERE
Wet
Ones
ANTIBACTERIAL
HAND WIPE
Lavender Scent
KILLS 99.99% OF GERMS*
8 Hour Moisturization
*Effective at killing 99.99%
of many common harmful
bacteria in as little as
15 seconds
1 WIPE
actual size

Pocket Size Singles
Tough on Germs
Gentle on Skin
8-hour
Moisturization
Hypoallergenic
Paraben Free
24 INDIVIDUALLY
WRAPPED WIPES

INGREDIENTS AND APPEARANCE

WET ONES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-365
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
ALCOHOL (UNII: 3K9958V90M)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-365-24	24 in 1 BOX; Type 0: Not a Combination Product	02/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/01/2024

Labeler - Edgewell Personal Care Brands LLC (151179769)