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AQUACIL

Medically reviewed by Drugs.com. Last updated on Oct 20, 2021.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 100mg in 100mL
Labeler: Inopak, Ltd
NDC Code: 58575-170

Inopak - Aquacil - 170

Drug Facts
Active Ingredient

Benzalkonium Chloride 0.1% W/W

Purpose

Antiseptic

Keep out of reach of children

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

Uses
  • Handwash to help reduce bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

Warnings
  • For external use only.
  • Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

irritation and redness develop or if condition persists for more than 72 hours.

Directions
  • Pump sufficient amount of foam into palm of hand.
  • Wet all surfaces of both hands thoroughly with product, including the area under the fingernails and rub until dry.

Inactive Ingredients

Cetrimonium chloride, laurtrimonium chloride, phenoxyethanol, stearalkonium chloride, water

AQUACIL ™
INSTANT FOAMING HAND SANITIZER

KILLS 99.9% OF GERMS
Alcohol Free Formula

Benzalkonium Chloride 0.1%
For Use Without Water

biocentris PHARMACEUTICALS
888-497-4375
info@biocentrispharmaceuticals.com
www.biocentrispharmaceuticals.com

50 ml

BIO-5075-480

AQUACIL 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58575-170
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE100 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CETRIMONIUM CHLORIDE 
LAURTRIMONIUM CHLORIDE 
PHENOXYETHANOL 
STEARALKONIUM CHLORIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:58575-170-0250 mL in 1 BOTTLE, PUMP
2NDC:58575-170-80237 mL in 1 BOTTLE, PUMP
3NDC:58575-170-18473 mL in 1 BOTTLE, PLASTIC
4NDC:58575-170-373785 mL in 1 BOTTLE
5NDC:58575-170-101000 mL in 1 CARTRIDGE
6NDC:58575-170-121000 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2013
Labeler - Inopak, Ltd (194718243)
Registrant - Inopak, Ltd (194718243)
Establishment
NameAddressID/FEIOperations
Inopak, Ltd194718243manufacture(58575-170)

Document Id: a0a4a0aa-e449-4c83-a78f-769175218834
Set id: ad513dd9-5c44-4c64-bb97-6ced49aae02a
Version: 7
Effective Time: 20191030
 
Inopak, Ltd

Further information

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

Medical Disclaimer