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

Deb InstantFOAM PURE Non-Alcohol Hand Sanitizer by

Drug Labeling and Warnings

Deb InstantFOAM PURE Non-Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc., Deb Worldwide Healthcare 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, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLINONE, MAGNESIUM CHLORIDE, METHYLISOTHIAZOLINONE

PRINCIPAL DISPLAY PANEL

deb stoko

Deb InstantFOAM PURE

Non-Alcohol - Dye & Fragrance Free Hand Sanitizer

Antiséptico para manos en espuma - sin alcohol, sin colorante y sin perfume

DISINFECT

NON-ALCOHOL

DCN8901/0415

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 PURE NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-150
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-150-01	0.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/15/2015	12/01/2022
2	NDC: 11084-150-40	0.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/15/2015	12/01/2022
3	NDC: 11084-150-27	1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/15/2015	12/01/2022
4	NDC: 11084-150-12	1.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/15/2015	12/01/2022
5	NDC: 11084-150-99	1230 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 1: Convenience Kit of Co-Package	04/15/2015	12/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/15/2015	12/01/2022

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb USA, Inc.		078805627	manufacture(11084-150)

Establishment
Name	Address	ID/FEI	Business Operations
Deb Worldwide Healthcare Inc.		205662831	repack(11084-150)