InstantFOAM non-alcohol hand sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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InstantFOAM non-alcohol hand sanitizer

Deb USA, Inc.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient

Benzalkonium Chloride, 0.13%

Purpose

Purpose

Antibacterial

Uses

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

Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Fragrance, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200)

deb

InstantFOAM

non-alcohol hand sanitizer

refreshing

no water required

use anywhere, any time

use everyday

Kills 99.99% of common germs

deb foam technology

56827-01-116

1 Liter - 33.8 Fluid Ounces

InstantFOAM non-alcohol hand sanitizer

InstantFOAM non-alcohol hand sanitizer

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11084-057
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mL

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
ANHYDROUS CITRIC ACID
D&C RED NO. 33
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-057-01 47 in 1 BOTTLE, PUMP
2 NDC:11084-057-05 3780 in 1 BOTTLE, PLASTIC
3 NDC:11084-057-20 2000 in 1 BOTTLE, PLASTIC
4 NDC:11084-057-27 1000 in 1 BOTTLE, PLASTIC
5 NDC:11084-057-40 400 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-01-01


Safe-T-Fresh Alcohol Free Hand Sanitizer

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11084-129
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mL

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
ANHYDROUS CITRIC ACID
D&C RED NO. 33
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-129-27 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-01-01


Drummond Aero Instant

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11084-112
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mL

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
ANHYDROUS CITRIC ACID
D&C RED NO. 33
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-112-01 47 in 1 BOTTLE, PUMP
2 NDC:11084-112-27 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-01-01


United Labs Instant Foam

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11084-113
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mL

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
ANHYDROUS CITRIC ACID
D&C RED NO. 33
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-113-27 400 in 1 BOTTLE, PUMP
2 NDC:11084-113-40 47 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-01-01


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