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 Onpoinr, Inc, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

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

Warnings

For external use only-hands

Flammable. Keep away from heat and flame

When using this product

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

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

Other information

do not store above 105⁰  may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin,
isopropyl myristate, propylene glycol, tocopheryl acetate, water, yellow 5

SPL UNCLASSIFIED SECTION

Not manufactured or distributed by GOJO Industries, owner of the registered trademark Purell

Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Distributed by: Onpoint, Inc
2 Paragon Drive,
Montvale, NJ 07645

PRINCIPAL DISPLAY PANEL

Live Better
Waterless Hand Sanitizer With Aloe
Kills 99.99% of Germs
8 FL OZ (236 mL)

203.000/203AB

INGREDIENTS AND APPEARANCE

WATERLESS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51143-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	.65 mL  in 100 L

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51143-203-34	.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2011

Labeler - Onpoinr, Inc (001367366)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(51143-203)