Stay Clean Foam Hand Sanitizer

Dosage form: liquid
Ingredients: Benzalkonium Chloride 0.13mL in 100mL
Labeler: Byotrol, Inc.
NDC Code: 42719-345

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient                                       Purpose

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

Directions

Pump a small amount of foam onto hands

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

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


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)

STAY CLEAN FOAM HAND SANITIZER 
hand sanitizer liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42719-345
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride0.13 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Dimethicone 
Water 
Packaging
#Item CodePackage Description
1NDC:42719-345-50500 mL in 1 BOTTLE
2NDC:42719-345-51210 mL in 1 BOTTLE
3NDC:42719-345-831000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33309/18/2009
Labeler - Byotrol, Inc. (084600340)
Establishment
NameAddressID/FEIOperations
Bayscience Formulators Inc.162930544manufacture

Revised: 10/2009
 
Byotrol, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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