Byotrol Antibacterial Foaming Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Byotrol Antibacterial Foaming Hand Sanitizer

Byotrol, Inc.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Purpose

Antimicrobial

Uses

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes.

In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

if swallowed, get medical help or contact a Poison Control Center right away.











Inactive ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Glycereth-17 Cocoate, Dihydroxyethyl Cocamine Oxide, Polyaminopropyl Biguanide, C8-10-Alkyl Polyglucoside, C12-15 Pareth-7, Citric Acid, Dimethicone

100%

Hygeine

Revolution

Byotrol

Alcohol Free

Kills Germs

Antibacterial Foaming

Hand Sanitizer

Powerful

No other FDA compliant hand antiseptic claims more.

Long Lasting

Foaming formula lasts, increasing wet contact time, to deliver the persistent performance Byotrol is known for.

Gentle

Alcohol Free Formula is hard on germs and soft on hands.

byotrol

Net Contents: 42.26 fl.Oz. (1,250ml)

Byotrol Antibacterial Foaming Hand Sanitizer


Byotrol Antibacterial Foaming Hand Sanitizer

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42719-346
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 1.3 mg

Inactive Ingredients

Ingredient Name Strength
water
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
GLYCERETH-17 COCOATE
dihydroxyethyl cocamine oxide
POLIHEXANIDE
C12-15 PARETH-7
CITRIC ACID MONOHYDRATE
DIMETHICONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42719-346-50 500 in 1 BOTTLE
2 NDC:42719-346-51 210 in 1 BOTTLE
3 NDC:42719-346-99 50 in 1 BOTTLE
4 NDC:42719-346-06 1250 in 1 CARTRIDGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2013-03-08


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.