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Woodwards HandClens Foaming Sanitizer

Medically reviewed on October 20, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Pacific World Corporation
NDC Code: 60193-202

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

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, Fragrance, Ext. Violet 2 (CI 60730), Green 5 (CI 61570).

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

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 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60193-202
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 
D&C GREEN NO. 5 
EXT. D&C VIOLET NO. 2 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:60193-202-01236 mL in 1 BOTTLE, PUMP
2NDC:60193-202-031000 mL in 1 CARTRIDGE
3NDC:60193-202-051800 mL in 1 BOTTLE, PUMP
4NDC:60193-202-0750 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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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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