I.C. HAND SANITIZER- benzalkonium chloride aerosol, foam

I.C. Hand Sanitizer by

Drug Labeling and Warnings

I.C. Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by R&R Lotion, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

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

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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

Directions

• Pump a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together briskly until dry.

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid

Questions or Comments?

Call (480) 443-9255
or visit RRlotion.com

PRINCIPAL DISPLAY PANEL - 591 ml Bottle Label

R&R LOTION
I.C. HAND SANITIZER™

"ALCOHOL FREE"
20 FL. OZ. (591ML) e

INGREDIENTS AND APPEARANCE

I.C. HAND SANITIZER 
benzalkonium chloride aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-401
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Laurtrimonium Chloride (UNII: A81MSI0FIC)
Dihydroxyethyl Cocamine Oxide (UNII: 8AR51R3BL5)
Glycereth-17 Cocoate (UNII: 3057VPT0KC)
Citric Acid Monohydrate (UNII: 2968PHW8QP)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-401-12	591 mL in 1 BOTTLE, PUMP
2	NDC: 59555-401-11	3785 mL in 1 BOTTLE, PUMP
3	NDC: 59555-401-13	50 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	06/15/2014

Labeler - R&R Lotion, Inc. (062979000)