ANTIBACTERIAL LIQUID HAND- triclosan liquid

Antibacterial Liquid Hand by

Drug Labeling and Warnings

Antibacterial Liquid Hand by is a Otc medication manufactured, distributed, or labeled by OnPoint, Inc, Vi Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Triclosan 0.115%

Purpose
Antibacterial

INDICATIONS & USAGE

Uses for handwashing to decrease bacteria on the skin

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions  Wet hands  Apply palmful to hands  Scrub thoroughly Rinse

INACTIVE INGREDIENT

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

ADVERSE REACTIONS

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

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL LIQUID HAND 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51143-541
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	.115 kg  in 100 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51143-541-93	1.18 L in 1 BOTTLE, PLASTIC
2	NDC: 51143-541-96	.221 L in 1 BOTTLE, PLASTIC
3	NDC: 51143-541-97	1.89 L in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/30/2009

Labeler - OnPoint, Inc (001367366)

Registrant - Vi Jon (150931459)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		150931459	manufacture