STAY CLEAN FOAM HAND SANITIZER- hand sanitizer liquid

Stay Clean Foam Hand Sanitizer by

Drug Labeling and Warnings

Stay Clean Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Byotrol, Inc., Bayscience Formulators Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                       Purpose

Benzalkonium Chloride 0.13%....................Antimicrobial

INDICATIONS & USAGE

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

WARNINGS

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 conditions 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.

DOSAGE & ADMINISTRATION

Directions

Pump a small amount of foam onto hands

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

INACTIVE INGREDIENT

Inactive ingredients:

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, polyaminopropyl biguanide, dimethicone, C12-C15 pareth-7, alkyl polyglucoside

PRINCIPAL DISPLAY PANEL

Stay Clean Foam Sanitizer

byotrol

Kills MRSA

Kills 99.9% of common germs that may cause illness, after a 15 second wet time

New and Improved Formula

Alcohol and Fragrance Free

Case Quantity 8

Not For Individual Resale

Moisturizing and conditioning formula

Net contents: 33.8 fl. oz. (1,000ml)

INGREDIENTS AND APPEARANCE

STAY CLEAN FOAM HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42719-345
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.13 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Dimethicone (UNII: 92RU3N3Y1O)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42719-345-50	500 mL in 1 BOTTLE
2	NDC: 42719-345-51	210 mL in 1 BOTTLE
3	NDC: 42719-345-83	1000 mL in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	09/18/2009

Labeler - Byotrol, Inc. (084600340)

Establishment
Name	Address	ID/FEI	Business Operations
Bayscience Formulators Inc.		162930544	manufacture