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WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE

Medically reviewed on October 20, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Pacific World Corporation
NDC Code: 60193-203

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.

Woodward's HandClens® Foaming Sanitizer & Lotion Color & Fragrance Free

Drug Facts

Active ingredient

Benzalkonium Chloride, 0.13%

Purpose

Antiseptic Hand Sanitizer

Use

for hand sanitizing to decrease bacteria on the skin

Warnings
  • For external use only

When using this product
  • Avoid contact with eyes. In case of eye contact, flush with water

  • Stop use and ask a doctor if rash or irritation develops and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions
  • Use enough foam to cover your hands
  • Rub hands together briskly until dry

Other information
  • Do not store above 110°F (40°C)
  • You may report questions or adverse reaction from using this product to 1(541)-476-3178, 8 am to 5 pm (M–F), PST

Inactive ingredients

Water, Cocamidopropylamine Oxide, Didecyldimonium Chloride, Allantoin, Propylene Glycol, Cetrimonium Chloride, Cocamidopropyl Betaine, Sodium Hydroxide, Diazolidinyl Urea, Methylparaben, Propylparaben.

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

Fragrance-Free
Color-Free

2 in 1
Sanitizer & Lotion

WOODWARD'S
HandClens
®

Foaming Sanitizer & Lotion
Alcohol-Free*• Non-Flammable

Softens Hands with Each Use!

Kills 99.99%
of Germs

1.7 FL OZ (50 mL)

WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60193-203
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
DIDECYLDIMONIUM CHLORIDE 
METHYLPARABEN 
PROPYLPARABEN 
PROPYLENE GLYCOL 
DIAZOLIDINYL UREA 
ALLANTOIN 
COCAMIDOPROPYLAMINE OXIDE 
CETRIMONIUM CHLORIDE 
COCAMIDOPROPYL BETAINE 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:60193-203-01236 mL in 1 BOTTLE, PUMP
2NDC:60193-203-031000 mL in 1 CARTRIDGE
3NDC:60193-203-051800 mL in 1 BOTTLE, PUMP
4NDC:60193-203-0750 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A05/01/2014
Labeler - Pacific World Corporation (089693097)

 
Pacific World Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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