INSTANT FOAM NON-ALCOHOL HAND SANITIZER- benzalkonium chloride liquid 
SC Johnson Professional USA, Inc.

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Instant Foam™ Non-alcohol Hand Sanitizer

Drug Facts

Active ingredient

Benzalkonium Chloride, 0.13%

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease

Warnings

For external use only

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.

Inactive ingredients

Aqua (Water), Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Citric Acid, Cocamidopropyl Betaine, Lauramine Oxide, Parfum (Fragrance), Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Blue 1 (CI 42090), Red 33 (CI 17200)

PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label

SCJ PROFESSIONAL
A Family Company™

NDC 11084-301-27

InstantFOAM™ Non-Alcohol

HAND SANITIZER
Alcohol-Free FOAM Hand Sanitizer - Fragranced

PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label
INSTANT FOAM NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
EDETATE SODIUM (UNII: MP1J8420LU)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-301-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
2NDC:11084-301-97296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/202012/31/2024
3NDC:11084-301-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/202012/31/2024
4NDC:11084-301-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/202312/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drug505G(a)(3)04/15/201512/31/2024
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
APEX International, Inc.015226132MANUFACTURE(11084-301)

Revised: 12/2024
Document Id: 5c0f1dee-12f6-4a7a-9c97-60aefc4540e4
Set id: 5c2c222d-4392-4b90-b982-90d576a8cbe1
Version: 5
Effective Time: 20241217
 
SC Johnson Professional USA, Inc.