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Antibacterial Liquid Hand by OnPoint, Inc

Medically reviewed on November 20, 2017

Dosage form: liquid
Ingredients: TRICLOSAN .115kg in 100L
Labeler: OnPoint, Inc
NDC Code: 51143-541

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
Triclosan 0.115%

Purpose
Antibacterial

Uses for handwashing to decrease bacteria on the skin

Warnings
For external use only
.

When using this product • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

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

Directions  •Wet hands  •Apply palmful to hands  •Scrub thoroughly •Rinse

Inactive ingredients water, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, sodium chloride, decyl glucoside, fragrance, DMDM hydantoin, PEG-120 methyl glucose dioleate, cocamide MEA, citric acid, tetrasoidum EDTA, polyquaternium-7, PEG-7 glyceryl cocoate, D+C red no. 33, FD+C, blue no. 1

Distributed by OnPoint, Inc
2 Paragon Drive, Montvale, NJ 07645

MARKET SPA
ANTIBACTERIAL
LIQUID HAND SOAP
CLEAR FORMULA
7.5 FL OZ (221 mL)

ANTIBACTERIAL LIQUID HAND 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51143-541
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN.115 kg  in 100 L
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURETH SULFATE 
SODIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
SODIUM CHLORIDE 
DMDM HYDANTOIN 
PEG-120 METHYL GLUCOSE DIOLEATE 
Packaging
#Item CodePackage Description
1NDC:51143-541-931.18 L in 1 BOTTLE, PLASTIC
2NDC:51143-541-96.221 L in 1 BOTTLE, PLASTIC
3NDC:51143-541-971.89 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/30/2009
Labeler - OnPoint, Inc (001367366)
Registrant - Vi Jon (150931459)
Establishment
NameAddressID/FEIOperations
Vi Jon150931459manufacture

 
OnPoint, Inc

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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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