WATERLESS HAND SANITIZER- alcohol gel

Waterless Hand Sanitizer by

Drug Labeling and Warnings

Waterless Hand Sanitizer 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

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Warnings

For external use only-hands

Flammable.

Keep away from heat or flame

When using this product

• keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale of ingest

Stop use and ask a doctor if

skin irritation develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Inactive ingredients

 benzophenon-4, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Adverse reaction

DISTRIBUTED BY ONPOINT, INC

2 PARAGON DRIVE

MONTVALE, NJ 07645

SPL UNCLASSIFIED SECTION

Effective at eliminating over 99.99% of many common harmful germs and bacteria in as little as 15 seconds Made in the USA with US and foreign components

PRINCIPAL DISPLAY PANEL

LiveBetter

Waterless

Hand

Sanitizr

ORIGINAL

• KILLS 99.99% OF GERMS

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

WATERLESS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51143-545
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	.62 kg  in 100 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51143-545-16	.06 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/09/2009
2	NDC: 51143-545-24	.24 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/09/2009
3	NDC: 51143-545-45	.94 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/09/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/09/2009

Labeler - ONPOINT, INC (001367366)

Registrant - Vi Jon (150931459)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		150931459	manufacture(51143-545)