WET ONES- benzethonium chloride swab 
Energizer Personal Care LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

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 throroughly 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

Children under 2 years

Inactive Ingredients

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

Questions or Comments?

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

Principle Display Panel

FRESH SCENT

WET ONES

ANTIBACTERIAL

HAND WIPES

Kills 99.99% of Germs

cleans better than hand sanitizers

hypoallergenic

35 wipes

Wet Ones Fresh Scent 35 canister

WET ONES 
benzethonium chloride swab
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63354-998
Route of Administration TOPICAL DEA Schedule     
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
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
QUATERNIUM-52 (UNII: 588EQF3H1P)  
SODIUM CAPRYLOAMPHOPROPIONATE (UNII: W9H6IT16GQ)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63354-998-15 15 in 1 POUCH
2 NDC:63354-998-20 20 in 1 POUCH
3 NDC:63354-998-24 24 in 1 PACKAGE
4 NDC:63354-998-26 26 in 1 PACKAGE
5 NDC:63354-998-28 28 in 1 POUCH
6 NDC:63354-998-35 35 in 1 POUCH
7 NDC:63354-998-36 35 in 1 CANISTER
8 NDC:63354-998-40 40 in 1 CANISTER
9 NDC:63354-998-42 42 in 1 CANISTER
10 NDC:63354-998-48 48 in 1 CANISTER
11 NDC:63354-998-14 144 in 1 PACKAGE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 10/01/2007
Labeler - Energizer Personal Care LLC (021718141)

Revised: 12/2012
Document Id: 61d7554e-610b-410e-a203-a52abd09aa80
Set id: 007bcc58-e10e-4c8f-a537-dec23c89987e
Version: 1
Effective Time: 20121228
 
Energizer Personal Care LLC