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Clementine Hand Sanitizer

Medically reviewed on December 30, 2016.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Mangiacotti, Inc
NDC Code: 42926-162

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.

Clementine hand sanitizer spray

Clementine hand sanitizer spray


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

Spray a small amount 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, fragrance with essential oils

Clementine hand sanitizer spray 0.5oz/15ml (42926-162-15)

CLEMENTINE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42926-162
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CETRIMONIUM CHLORIDE 
LAURTRIMONIUM CHLORIDE 
DIHYDROXYETHYL COCAMINE OXIDE 
GLYCERETH-17 COCOATE 
CITRIC ACID MONOHYDRATE 
Packaging
#Item CodePackage Description
1NDC:42926-162-151 BOTTLE, SPRAY in 1 PACKAGE
115 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/14/2014
Labeler - Mangiacotti, Inc (078850804)
Establishment
NameAddressID/FEIOperations
Precise Packaging LLC079904428manufacture(42926-162)

 
Mangiacotti, 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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