WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE- benzalkonium chloride liquid

WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE by

Drug Labeling and Warnings

WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE by is a Otc medication manufactured, distributed, or labeled by Pacific World Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60193-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
ALLANTOIN (UNII: 344S277G0Z)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60193-203-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 60193-203-03	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
3	NDC: 60193-203-05	1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC: 60193-203-07	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	05/01/2014

Labeler - Pacific World Corporation (089693097)