WET ONES- benzethonium chloride swab

Wet Ones by

Drug Labeling and Warnings

Wet Ones 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

Benzethonium Chloride 0.3%

Purpose

Antibacterial

Use

decrease 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 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., PEG-8 Dimethicone, Phenoxyethanol, Quaternium-52, Potassium Sorbate, Sodium Capryloamphopropionate, Methylparaben, Citric Acid, Disodium EDTA, Fragrance, Ethylparaben, PEG-60 Lanolin, Propylparaben, Aloe Barbadensis Leaf Juice

Questions or Comments?

Call 1-866-WET-111S; (1-866-938-1117), M-F

PDP

FRESH

SCENT

Wet

Ones

ANTIBACTERIAL

HAND WIPES

Kills 99.99% of Germs

cleans better than

hand sanitizers

hypoallergenic

INGREDIENTS AND APPEARANCE

WET ONES 
benzethonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63354-998
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.3   in 100

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM CAPRYLOAMPHOPROPIONATE (UNII: W9H6IT16GQ)
METHYLPARABEN (UNII: A2I8C7HI9T)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PEG-60 LANOLIN (UNII: K2OI1D27ET)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)
QUATERNIUM-52 (UNII: 588EQF3H1P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLPARABEN (UNII: 14255EXE39)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63354-998-15	15 in 1 POUCH; Type 0: Not a Combination Product	10/01/2007	03/01/2018
2	NDC: 63354-998-20	20 in 1 POUCH; Type 0: Not a Combination Product	10/01/2007
3	NDC: 63354-998-24	24 in 1 PACKAGE; Type 0: Not a Combination Product	10/01/2007
4	NDC: 63354-998-26	26 in 1 PACKAGE; Type 0: Not a Combination Product	10/01/2007	03/01/2018
5	NDC: 63354-998-28	28 in 1 POUCH; Type 0: Not a Combination Product	10/01/2007
6	NDC: 63354-998-35	35 in 1 POUCH; Type 0: Not a Combination Product	10/01/2007	03/01/2018
7	NDC: 63354-998-36	35 in 1 CANISTER; Type 0: Not a Combination Product	10/01/2007	03/01/2018
8	NDC: 63354-998-40	40 in 1 CANISTER; Type 0: Not a Combination Product	10/01/2007
9	NDC: 63354-998-42	42 in 1 CANISTER; Type 0: Not a Combination Product	10/01/2007	03/01/2018
10	NDC: 63354-998-48	48 in 1 CANISTER; Type 0: Not a Combination Product	10/01/2007
11	NDC: 63354-998-14	144 in 1 PACKAGE; Type 0: Not a Combination Product	10/01/2007
12	NDC: 63354-998-65	65 in 1 CANISTER; Type 0: Not a Combination Product	10/01/2007

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2007

Labeler - Edgewell Personal Care Brands LLC (151179769)