DEB INSTANTFOAM NON-ALCOHOL- benzalkonium chloride 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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Drug Facts

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%   

Purpose

Antibacterial

Uses

for hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply one shot to dry hands, rub into skin

no rinsing required

Inactive ingredients

ALOE BARBADENSIS LEAF JUICE, AQUA (WATER), CITRIC ACID, COCAMIDOPROPYL BETAINE, LAURAMINE OXIDE, MAGNESIUM CHLORIDE, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, PARFUM (FRAGRANCE), PROPYLENE GLYCOL, TETRASODIUM EDTA, BLUE 1 (CI 42090), RED 33 (CI 17200)

deb stoko

Deb InstantFOAM(R) Non-Alcohol

Fragranced Hand Sanitizer

Antiseptico para manos en espuma - sin alcohol y con perfume

SANITIZE

NON-ALCOHOL

Deb USA, Inc. Charlotte,

NC 28217. 1-800-248-7190

www.debgroup.com

Made in USA

1 L

(33.8 fl oz)

DCN8900/0716

56827-DCN8900 InstantFOAM Non-Alcohol-1L-V8.jpg

56827-DCN8900 InstantFOAM Non-Alcohol-1L-V8.jpg

DEB INSTANTFOAM NON-ALCOHOL 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-002
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
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:11084-002-0147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/07/201612/01/2022
2NDC:11084-002-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/07/201609/20/2023
3NDC:11084-002-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/07/201610/11/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/07/201609/20/2023
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300Manufacture(11084-002)

Revised: 12/2022
Document Id: 983f8bf5-668b-4799-b7df-2371116839cd
Set id: 75976c28-7d35-4a3b-8933-c9b5a5c88fd4
Version: 3
Effective Time: 20221222
 
SC Johnson Professional USA, Inc.