WOODWARDS HANDCLENS FOAMING SANITIZER COLOR AND FRAGRANCE FREE- 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 Sanitizer

Uses

• When soap and water are not available.
• Kills germs and helps prevent infections in minor cuts and abrasions.

Warnings

• Do not use in eyes,ears or mouth. In case of eye contact, flush with water immediately.

• Stop use and ask a doctor if rash or irritation occurs or if condition persists.

• Keep out of reach of children under 2 years of age.

Directions

• Apply as needed and rub into skin.
• No rinsing necessary.

Inactive Ingredients

Water, Didecyldimonium Chloride, Methylparaben, Propylparaben, Propylene Glycol, Diazolidinyl Urea, Allantoin, Cocamidopropylamine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Triethanolamine, Citric Acid

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

Color-Free
Fragrance-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

8 FL OZ (236 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: 60193-201
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)
TROLAMINE (UNII: 9O3K93S3TK)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60193-201-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 60193-201-03	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
3	NDC: 60193-201-05	1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC: 60193-201-07	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	06/03/2013

Labeler - Pacific World Corporation (089693097)