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  4. NDC Product Code: 68040-706 Aloquin

NDC 68040-706 Aloquin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68040-706?
  5. Aloquin Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68040-706
Proprietary Name:
Aloquin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Primus Pharmaceuticals
Labeler Code:
68040
Product Label ID:
179b8b28-c76b-4686-a04c-6b2f90056de9
Start Marketing Date: [9]
07-06-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)

Code Structure Chart

Product Details

What is NDC 68040-706?

The NDC code 68040-706 is assigned by the FDA to the product Aloquin which is product labeled by Primus Pharmaceuticals. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 68040-706-01 1 g in 1 packet , 68040-706-08 10 packet in 1 box / 1 g in 1 packet, 68040-706-16 1 tube in 1 box / 60 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Aloquin?

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.

Which are Aloquin UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Aloquin?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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]

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".