Wet Ones Antibacterial Hand Wipes Spring Bliss by Edgewell Personal Care Brands LLC

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]

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

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

WET ONES ANTIBACTERIAL HAND WIPES SPRING BLISS 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-905
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 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-905-25	25 g in 1 POUCH; Type 0: Not a Combination Product	07/25/2022	04/30/2023
2	NDC: 63354-905-50	50 g in 1 POUCH; Type 0: Not a Combination Product	07/25/2022	06/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/25/2022	06/30/2023

Labeler - Edgewell Personal Care Brands LLC (151179769)

Revised: 9/2023

Document Id: 065c12b7-b8a7-f691-e063-6294a90a7b9b

34390-5

Set id: e4a57b08-a6e1-cf82-e053-2995a90a8ea3

Version: 2

Effective Time: 20230927