WOODWARDS HANDCLENS FOAMING SANITIZER- benzalkonium chloride liquid

Woodwards HandClens Foaming Sanitizer by

Drug Labeling and Warnings

Woodwards HandClens Foaming Sanitizer 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, 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)

INGREDIENTS AND APPEARANCE

WOODWARDS HANDCLENS FOAMING SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60193-202
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)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60193-202-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 60193-202-03	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
3	NDC: 60193-202-05	1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC: 60193-202-07	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)