A-QUAT LIQ

Main information

  • Trade name:
  • A-QUAT LIQ LIQUID
  • Dosage:
  • 1.05%; 1.05%; 2.80%; 2.10%
  • Pharmaceutical form:
  • LIQUID
  • Composition:
  • DIDECYL DIMETHYL AMMONIUM CHLORIDE 1.05%; DIOCTYL DIMETHYL AMMONIUM CHLORIDE 1.05%; BENZALKONIUM CHLORIDE 2.80%; OCTYL DECYL DIMETHYL AMMONIUM CHLORIDE 2.10%
  • Administration route:
  • DISINFECTANT (Food Premises)
  • Units in package:
  • 4/20/205L
  • Prescription type:
  • OTC
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical

Documents

Localization

  • Available in:
  • A-QUAT LIQ LIQUID
    Canada
  • Language:
  • English

Therapeutic information

  • Therapeutic area:
  • DISINFECTANTS (FOR AGENTS USED ON OBJECT)
  • Product summary:
  • Active ingredient group (AIG) number: 0414758005; AHFS: 38:00.00

Other information

Status

  • Source:
  • Health Canada
  • Authorization status:
  • APPROVED
  • Authorization number:
  • 00799408
  • Authorization date:
  • 05-03-2010
  • Last update:
  • 27-11-2018

21-11-2018

Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex

Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex

Fresenius Kabi USA is voluntarily recalling 163 lots of Sodium Chloride Injection, USP, 0.9%, 10 mL fill in a 10 mL vial and Sodium Chloride Injection, USP, 0.9%, 20 mL fill in a 20 mL vial to the user level. The product insert states that stoppers for both the 10mL and the 20mL vials do not contain natural rubber latex; the tray label for the two vial sizes and the vial label for the 20mL vial also state that the stoppers do not contain latex. The product is being recalled because the stoppers contain n...

FDA - U.S. Food and Drug Administration

16-10-2018

Modification of the existing maximum residue levels for mepiquat in cotton seeds and animal commodities

Modification of the existing maximum residue levels for mepiquat in cotton seeds and animal commodities

Published on: Mon, 15 Oct 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant, BASF SE, submitted an application to the competent national authority in Greece to modify the existing maximum residue level (MRL) for the active substance mepiquat in cotton seeds. The data submitted in support of the application were found to be sufficient to derive a MRL proposal for cotton seeds and the previously derived MRL proposals for animal commodities were found to be stil...

Europe - EFSA - European Food Safety Authority Publications

7-9-2018

SCA Pharmaceuticals LLC. Issues Voluntary Nationwide Recall of Furosemide 100 mg in 0.9% Sodium Chloride due to Presence of Precipitate

SCA Pharmaceuticals LLC. Issues Voluntary Nationwide Recall of Furosemide 100 mg in 0.9% Sodium Chloride due to Presence of Precipitate

, SCA Pharmaceuticals LLC (“SCA Pharma”) is voluntarily recalling 7 lots of the injectable product Furosemide 100 mg in 0.9% Sodium Chloride 100 mg bag to the consumer level. This product is being recalled for visible particulate matter believed to be furosemide precipitate.

FDA - U.S. Food and Drug Administration

22-3-2018

Lutetium (<sup>177</sup> Lu) chloride

Lutetium (<sup>177</sup> Lu) chloride

Lutetium (177 Lu) chloride (Active substance: Lutetium (177Lu) chloride) - Centralised - Art 28 - (PSUR - Commission Decision (2018)1902 of Thu, 22 Mar 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10391/201706

Europe -DG Health and Food Safety