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Microban 80

Medically reviewed on Jan 12, 2018

Dosage form: gel
Ingredients: ALCOHOL 0.8L in 1L
Labeler: Noveko Inc
NDC Code: 49955-680

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.

Active ingredient Purpose

80% V/V Ethyl alcohol.....Antiseptic

Uses

for handwashing to decrease bacteria on the skin

recommended for repeated use

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use in the eyes.  In case of

contact, rinse eyes thoroughly

with water.

Discontinue use if irritation and

redness develop.

If condition persists

for more than 72 hours, consult

a doctor.

Keep out of reach of children.  If

swallowed, get medical help or contact

a Poison Control Center right away.

Directions

wet hands thoroughly with product

and allow to dry without wiping

supervise children in the use of this product

Other Information

avoid temperature over 110F

may discolor certain fabrics

harmful to wood finishes and plastics

Inactive ingredients

Water, Aloe vera, Carbomer, Tocopheryl acetate, Triethanolamine,

Glycerin.

Questions?

call 1 866 377-3030

weekdays, 9AM - 5PM EST

Enter section text here

ANTISEPTIC HAND SANITIZER

Microban 80% ALCOHOL

Unscented Antiseptic Hand Liquid

KILLS 99.9% OF GERMS

WATERLESS

Vitamin E and Aloe Vera enriched gel.

fl oz. (  L/mL)
MICROBAN 80 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49955-680
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.8 L  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL ACETATE, D- 
TROLAMINE 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:49955-680-101 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33311/18/2009
Labeler - Noveko Inc (205614519)

 
Noveko Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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