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Aloquin

ALOQUIN® gel (1.25% Iodoquinol and 1% Aloe Polysaccharides)

Approved
Approval ID

179b8b28-c76b-4686-a04c-6b2f90056de9

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 7, 2009

Manufacturers
FDA

Primus Pharmaceuticals

DUNS: 130834745

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Aloe Vera Leaf and Iodoquinol

PRODUCT DETAILS

NDC Product Code68040-706
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateOctober 7, 2009
Generic NameAloe Vera Leaf and Iodoquinol

INGREDIENTS (2)

Aloe Vera LeafActive
Quantity: 10 mg in 1 g
Code: ZY81Z83H0X
Classification: ACTIB
IodoquinolActive
Quantity: 12.5 mg in 1 g
Code: 63W7IE88K8
Classification: ACTIB

Drug Labeling Information

SPL UNCLASSIFIED SECTION

LOINC: 42229-5Updated: 10/7/2009

Rx ONLY
www.aloquin.com

Manufactured for:
Primus Pharmaceuticals, Inc.
Scottsdale, AZ 85251
www.primusrx.com

Manufactured by:
Sonar Products, Inc.
Carlstadt, NJ 07072

U.S. Patents #6,436,679; #6,271,214; #6,133,440; #5,925,357; #5,902,796; #5,708,038; #5,703,060; #5,468,737; other patents pending.
©2009 Primus Pharmaceuticals, Inc. All rights reserved.

ISS.0309 #15905

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 10/7/2009

DOSAGE AND ADMINISTRATION

Apply to affected areas 3-4 times daily or as directed by a physician. Follow your physician's directions regarding length of treatment after symptoms resolve.

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Aloquin - FDA Drug Approval Details