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

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Byotrol Hand Sanitizer

Advance Hygienics LLC

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.

Directions

Pump a small amount of foam onto hands.

Rub thoroughly over all surfaces of both hands.

Rub hands together briskly until dry.

Inactive ingredients:

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

byotrol

ANTIBACTERIAL FOAMING

HAND SANITIZER

ALCOHOL FREE  KILLS GERMS

POWERFUL

LONG LASTING

GENTLE

Net Contents: 1.69 fl. Oz. (50 ml)

Byotrol Hand Sanitizer


Byotrol Hand Sanitizer

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63002-002
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
CAPRYLYL GLUCOSIDE
C12-15 PARETH-7
CITRIC ACID MONOHYDRATE
DIMETHICONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63002-002-99 50 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2014-05-02


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