WET ONES ANTIBACTERIAL HAND WIPES FRESH SCENT- benzalkonium chloride swab

Wet Ones Antibacterial Hand Wipes Fresh Scent by

Drug Labeling and Warnings

Wet Ones Antibacterial Hand Wipes Fresh Scent 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 Ingredients

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 childre 2 years and over apply to hands 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, Disodium EDTA, Citric Acid, Fragrance, Aloe Barbadensis Leaf Juice

Primary Display Panel

Wet

Ones (R)

ANTIBACTERIAL

HAND WIPES

Fresh Scent

Kills 99.99% of Germs

Hypoallergenic Paraben Free

Fresh, Clean Feel

America's #1 Hand Wipe*

40

wipes

Fresh, Clean Feel

Wet

Ones(R)

ANTIBACTERIAL

HAND WIPES

Fresh Scent

Kills 99.99% of Germs

Hypoallergenic

WET LOCK(TM) SEAL

Keeps Wipes Moist

LIFT HERE

20

wipes

INGREDIENTS AND APPEARANCE

WET ONES ANTIBACTERIAL HAND WIPES FRESH SCENT 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-995
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

Inactive Ingredients
Ingredient Name	Strength
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-995-15	20 in 1 POUCH; Type 0: Not a Combination Product	04/27/2020
2	NDC: 63354-995-24	24 in 1 PACKET; Type 0: Not a Combination Product	04/27/2020
3	NDC: 63354-995-40	40 in 1 CANISTER; Type 0: Not a Combination Product	04/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2020

Labeler - Edgewell Personal Care Brands LLC (151179769)