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 TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:63354-998
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE0.3   in 100 
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
PEG-8 DIMETHICONE 
QUATERNIUM-52 
SODIUM CAPRYLOAMPHOPROPIONATE 
CITRIC ACID MONOHYDRATE 
EDETATE DISODIUM 
ALOE VERA LEAF 
PHENOXYETHANOL 
POTASSIUM SORBATE 
METHYLPARABEN 
ETHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63354-998-1515 in 1 POUCH
2NDC:63354-998-2020 in 1 POUCH
3NDC:63354-998-2424 in 1 PACKAGE
4NDC:63354-998-2626 in 1 PACKAGE
5NDC:63354-998-2828 in 1 POUCH
6NDC:63354-998-3535 in 1 POUCH
7NDC:63354-998-3635 in 1 CANISTER
8NDC:63354-998-4040 in 1 CANISTER
9NDC:63354-998-4242 in 1 CANISTER
10NDC:63354-998-4848 in 1 CANISTER
11NDC:63354-998-14144 in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/01/2007
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