WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS- 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 prodcut

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 medicial 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

Principal Display Panel

ANTIBACTERIAL

25

wipes label

ANTIBACTERIAL

Soft Texture

50

wipes

label2

Wet

Ones(r)

ANTIBACTERIAL

HAND WIPES

Spring Bliss

Touch of Aloe label3

Wet

Ones(r)

ANTIBACTERIAL HAND WIPES

Spring Bliss

Touch of Aloe

label

WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63354-905
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.11 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALCOHOL (UNII: 3K9958V90M)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CHAMOMILE (UNII: FGL3685T2X)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
EDETATE SODIUM (UNII: MP1J8420LU)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
BRONOPOL (UNII: 6PU1E16C9W)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63354-905-2525 g in 1 POUCH; Type 0: Not a Combination Product07/25/202204/30/2023
2NDC:63354-905-5050 g in 1 POUCH; Type 0: Not a Combination Product07/25/202206/30/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)07/25/202206/30/2023
Labeler - Edgewell Personal Care Brands LLC (151179769)

Revised: 9/2023
Document Id: 065c12b7-b8a7-f691-e063-6294a90a7b9b
Set id: e4a57b08-a6e1-cf82-e053-2995a90a8ea3
Version: 2
Effective Time: 20230927
 
Edgewell Personal Care Brands LLC