DEB INSTANTFOAM NON-ALCOHOL HAND SANITIZER- benzalkonium chloride liquid liquid

Deb InstantFOAM Non-Alcohol Hand Sanitizer by

Drug Labeling and Warnings

Deb InstantFOAM Non-Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA, Inc., SC Johnson Professional CA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

PRINCIPAL DISPLAY PANEL

deb stoko

Deb InstantFOAM

Non-Alcohol Hand Sanitizer

Antiséptico para manos en espuma - sin alcohol

DISINFECT

NON-ALCOHOL

DCN8900/0215

deb

Deb USA, Inc.  Charlotte, NC 28217

1-800-248-7190 www.debgroup.com

Made in USA

1 L

33.8 fl oz

INGREDIENTS AND APPEARANCE

DEB INSTANTFOAM NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-110-01	0.047 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	04/15/2015	12/01/2021
2	NDC: 11084-110-40	0.4 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	04/15/2015	12/01/2021
3	NDC: 11084-110-27	1 L in 1 BOTTLE, PLASTIC; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	04/15/2015	12/01/2021
4	NDC: 11084-110-99	1230 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 1: Convenience Kit of Co-Package	04/15/2015	12/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/15/2015	12/01/2021

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

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional USA, Inc.		078805627	manufacture(11084-110)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	repack(11084-110)