WET ONES ANTIBACTERIAL HAND WIPES LAVENDER SCENT- benzalkonium chloride swab

Wet Ones Antibacterial Hand Wipes Lavender Scent by

Drug Labeling and Warnings

Wet Ones Antibacterial Hand Wipes Lavender Scent by is a Otc medication manufactured, distributed, or labeled by Edgewell Personal Care Brands LLC, Sidney (1905 Progress Way). 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. 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

Wet
Ones
ANTIBACTERIAL
HAND WIPES
Lavender Scent
Tough On Dirt
Gentle on Skin
KILLS 99.99% OF COMMON BACTERIA
WET LOCK SEAL
Keeps Wipes Moist
LIFT HERE

8H Moisturization
20
wipes
Do Not Flush

Wet
Ones
ANTIBACTERIAL
HAND WIPES
Lavender Scent
Tough On Dirt
Gentle on Skin
KILLS 99.99% OF COMMON BACTERIA
8 Hour Moisturization
Do Not Flush
40
wipes

INGREDIENTS AND APPEARANCE

WET ONES ANTIBACTERIAL HAND WIPES LAVENDER SCENT 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-536
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  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-536-20	20 g in 1 POUCH; Type 0: Not a Combination Product	12/01/2022
2	NDC: 63354-536-40	40 g in 1 CANISTER; Type 0: Not a Combination Product	12/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/01/2022

Labeler - Edgewell Personal Care Brands LLC (151179769)