NDC Package 68040-706-08 Aloquin

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
68040-706-08
Package Description:
10 PACKET in 1 BOX / 1 g in 1 PACKET
Product Code:
Proprietary Name:
Aloquin
Usage Information:
Based on a review of a related drug by the National Research Council and subsequent FDA classification for that drug, the indications are as follows: "Possibly" Effective: Contact or atopic dermatitis; impetiginized eczema; nummular eczema; endogenous chronic infectious dermatitis; stasis dermatitis; pyoderma; nuchal eczema and chronic eczematoid otitis externa; acne urticata; localized or disseminated neurodermatitis; lichen simplex chronicus; anogenital pruritus (vulvae, scroti, ani); folliculitis; bacterial dermatoses; mycotic dermatoses such as tinea (capitis, cruris, corporis, pedis); monliasis; intertrigo. Final classification of the less-than-effective indications requires further investigation.
11-Digit NDC Billing Format:
68040070608
NDC to RxNorm Crosswalk:
  • RxCUI: 858356 - iodoquinol 1.25 % / aloe polysaccharide 1 % Topical Gel
  • RxCUI: 858356 - aloe polysaccharide 0.01 MG/MG / iodoquinol 0.0125 MG/MG Topical Gel
  • RxCUI: 858356 - aloe polysaccharide 1 % / iodoquinol 1.25 % Topical Gel
  • RxCUI: 858370 - Aloquin 1.25 % / 1 % Topical Gel
  • RxCUI: 858370 - aloe polysaccharide 0.01 MG/MG / iodoquinol 0.0125 MG/MG Topical Gel [Aloquin]
  • Labeler Name:
    Primus Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    07-06-2009
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68040-706-011 g in 1 PACKET
    68040-706-161 TUBE in 1 BOX / 60 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68040-706-08?

    The NDC Packaged Code 68040-706-08 is assigned to a package of 10 packet in 1 box / 1 g in 1 packet of Aloquin, labeled by Primus Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 68040-706 included in the NDC Directory?

    No, Aloquin with product code 68040-706 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Primus Pharmaceuticals on July 06, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68040-706-08?

    The 11-digit format is 68040070608. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-268040-706-085-4-268040-0706-08