FOAMING HAND WASH- triclosan liquid 
Onpoint, Inc

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.

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Drug Facts

Active ingredient

Triclosan 0.46%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only - hands only

When using this product

avoid contact with the eyes. If contact occurs, rinse eyes with water

Stop use and ask a doctor if

irritation or redness develops

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 thoroughly

Inactive ingredients

water, sodium laureth sulfate, glcerin, cocamidopropyl betaine, ammonium xylenesulfonate, fragrance, disodium phosphate, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, red 4, yellow 5

adverse reactions

DISTRIBUTED BY ONPOINT, INC

2 PARAGON DRIVE

MONTVALE, NJ 07645

ALL RIGHTS RESERVED

Principal display panel

America's Choice

antibacterial 

foaming hand wash

HELPS KILL HARMFUL GERMS

7.5 FL OZ (221 mL)

image description

FOAMING HAND WASH 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51143-962
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN.46 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51143-962-96221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/16/201204/28/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/16/201204/28/2017
Labeler - Onpoint, Inc (001367366)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon088520668manufacture(51143-962)

Revised: 5/2017
Document Id: 0594b7f5-60e0-43b9-a243-547420ae0523
Set id: bd57bd7c-a9c2-4564-9be7-b207d4054173
Version: 3
Effective Time: 20170501
 
Onpoint, Inc