ANTIBACTERIAL HAND- 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

ANTIBACTERIAL LIQUID HAND SOAP REFILL

Active ingredient

Triclosan 0.15%

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.

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

Inactive ingredients water, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, sodium chloride, decyl glucoside, glycerin, PEG-18 glyceryl oleate/cocoate, fragrance, cocamide MEA, DMDM hydantoin, tetrasodium EDTA, citric acid, yellow 5, red 4

This product is not manufactured or distributed by The Dial Corporation, distributor of Dial Gold antibacterial Soap

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

AMERICAS
CHOICE
ANTIBACTERIAL
LIQUID HAND SOAP
COMPARE TO DIAL
GOLD ANTIBACTERIAL SOAP
REFILL
64 FL OZ
(1.89 L)

image of principal display panel

ANTIBACTERIAL HAND
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51143-243
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.15 kg in 100 L

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-18 GLYCERYL OLEATE/COCOATE (UNII: VD2D270332)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51143-243-96	.221 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2009	03/14/2017
2	NDC:51143-243-97	1.89 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2009	03/14/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	02/26/2009	03/14/2017

Labeler - OnPoint, Inc (001367366)

Registrant - Vi-Jon (088520668)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon		088520668	manufacture(51143-243)

Revised: 4/2017

Document Id: 1cd4e11e-9aa2-4d87-abc5-f9a1cb22a5c4

Set id: ee1a658d-abe4-4a52-b6d8-15bdd98791a1

Version: 7

Effective Time: 20170428

OnPoint, Inc