CRISP APPLE HAND SANI- ethyl alcohol liquid

Crisp Apple Hand Sani by

Drug Labeling and Warnings

Crisp Apple Hand Sani by is a Otc medication manufactured, distributed, or labeled by Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

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

Warnings

For external use only

Flammable

 Keep away from heat and flame.

When using this product

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

Stop use

ask a doctor if skin irritation develops

Keep out of reach of children

 In case of accidental ingestion seek professional assistance 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 recommed for infants

Other Safety Information

• do not store above 105°F
• may discolor some fabrics
• harmful to wood finishes and plastics.

Inactive ingredients

benzophenone-4, carbomer, cellulose, fragrance, glycerin, hydroxypropyl methylcellulose, mannitol, red 4, red 40, retinyl palmitate, tocoperyl acetate, ultramarines, water

Adverse reaction

Distributed by: Vi-Jon

8515 Page Ave

St. Louis, MO 63114

663.001/663AA

principal display panel

crisp

apple

HandSani

HAND SANITIZER

germ-x

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

CRISP APPLE HAND SANI 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-663
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	585 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MANNITOL (UNII: 3OWL53L36A)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C RED NO. 40 (UNII: WZB9127XOA)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ULTRAMARINE BLUE (UNII: I39WR998BI)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-663-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/30/2012
2	NDC: 11344-663-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/30/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/30/2012

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		150931459	manufacture(11344-663)