INSTANTGEL HAND SANITIZER- alcohol liquid

InstantGEL Hand Sanitizer by

Drug Labeling and Warnings

InstantGEL Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., Vi-Jon Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

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

Warnings

For external use only

Flammable: Keep away from fire 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 or ingest.

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands thouroughly 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 105°F.
• May discolor certain fabrics or surfaces.
• Harmful to wood finishes and plactics.

Inactive ingredients

Water, Glyceryl Caprylate/Caprate, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Benzophenone-4

PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label

SCJ PROFESSIONAL
A Family Company™

NDC: 11084-027-27

InstantGEL™

HAND SANITIZER

Alcohol GEL hand sanitizer - Dye-free. Effective at eliminating more than
99.99% of many common harmful germs and bacteria in as little as
15 seconds. Leaves hands soft and fresh.

1L (33.8 fl oz)

Manufactured for:
SC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-800-248-7190
www.scjp.com

deb
SKIN CARE

Stock #: IGE1L
4000005015

L0018505SA

DRUG
FACTS

INGREDIENTS AND APPEARANCE

INSTANTGEL HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
SULISOBENZONE (UNII: 1W6L629B4K)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOCAPRYLOCAPRATE (UNII: G7515SW10N)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-027-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	12/01/2019

Labeler - SC Johnson Professional USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon Inc.		088520668	MANUFACTURE(11084-027)