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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

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68040-706
Product Classification
G
Generic Name
Aloe Vera Leaf and Iodoquinol
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 7, 2009
FDA Product Classification

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