DEB INSTANTFOAM NON-ALCOHOL- benzalkonium chloride liquid

Deb InstantFOAM Non-Alcohol by

Drug Labeling and Warnings

Deb InstantFOAM Non-Alcohol 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

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)

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

DEB INSTANTFOAM NON-ALCOHOL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-002-01	47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2016
2	NDC: 11084-002-40	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2016
3	NDC: 11084-002-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/07/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/07/2016

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

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional USA, Inc.		078805627	manufacture(11084-002)

Establishment
Name	Address	ID/FEI	Business Operations
SC Johnson Professional CA Inc.		203765300	repack(11084-002)