INSTANTGEL PURE- alcohol liquid 
SC Johnson Professional USA Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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InstantGEL™ PURE

Drug Facts

Active ingredient

Ethyl alcohol 78%v/v

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use
  • for when soap and water are not available

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

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)
  • May discolor certain fabrics or surfaces.
  • Harmful to wood finishes and plactics.

Inactive ingredients

Glycerin, Hydroxypropylcellulose, Water (Aqua)

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

SCJ PROFESSIONAL
A Family Company™

NDC 11084-181-17

InstantGEL™ PURE

HAND SANITIZER

Alcohol GEL
Hand Sanitizer
Dye-Free
Perfume-Free

4 fl oz
(118 mL)

deb
SKIN CARE

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label
INSTANTGEL PURE 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-181
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL78 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYPROPYL CELLULOSE (90000 WAMW) (UNII: UKE75GEA7F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-181-17118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/202007/17/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/202007/17/2023
Labeler - SC Johnson Professional USA Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
Fareva Morton Grove, Inc.116752326MANUFACTURE(11084-181)

Revised: 12/2022
Document Id: ebadd533-ae4b-4c61-9229-fc2284dbf563
Set id: 151da39b-2995-46f5-b9ff-e9ebc96ca634
Version: 2
Effective Time: 20221220
 
SC Johnson Professional USA Inc.