WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS- benzalkonium chloride swab

Wet Ones Antibacterial Hand Wipes Spring Bliss by

Drug Labeling and Warnings

Wet Ones Antibacterial Hand Wipes Spring Bliss 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 0.11%

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

(1-866-936-1117), M-F

Primary Display Panel

ANTIBACTERIAL

25

wipes

ANTIBACTERIAL

Soft Texture

50

wipes

Wet

Ones(r)

ANTIBACTERIAL

HAND WIPES

Spring Bliss

Touch of Aloe

Wet

Ones(r)

ANTIBACTERIAL HAND WIPES

Spring Bliss

Touch of Aloe

INGREDIENTS AND APPEARANCE

WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-904
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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-904-25	25 in 1 POUCH; Type 0: Not a Combination Product	01/08/2021
2	NDC: 63354-904-50	50 in 1 POUCH; Type 0: Not a Combination Product	01/08/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/08/2021

Labeler - Edgewell Personal Care Brands LLC (151179769)