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  4. NDC Product Code: 63102-105 Acticon

NDC 63102-105 Acticon

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63102-105?
  5. Acticon Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63102-105
Proprietary Name:
Acticon
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Actipharma, Inc.
Labeler Code:
63102
Product Label ID:
43fa98a5-02c7-4179-aae2-3994b2357bc6
Start Marketing Date: [9]
07-14-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 63102-105-16

Package Description: 480 mL in 1 PACKAGE

Product Details

What is NDC 63102-105?

The NDC code 63102-105 is assigned by the FDA to the product Acticon which is product labeled by Actipharma, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63102-105-16 480 ml in 1 package . 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 Acticon?

Uses:Temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upperrespiratory allergies:• relieves sinus congestion and pressure, helps decongest sinus openings and passages• restores freer breathing through the nose• runny nose • sneezing • itching of the nose or throat • itchy, watery eyes • nasal congestion

Which are Acticon UNII Codes?

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

  • DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS)
  • DEXBROMPHENIRAMINE (UNII: 75T64B71RP) (Active Moiety)
  • PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
  • PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)

Which are Acticon Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Acticon?

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: 1299143 - dexbrompheniramine maleate 1 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1299143 - dexbrompheniramine maleate 0.2 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1299143 - dexbrompheniramine maleate 1 MG / pseudoephedrine hydrochloride 30 MG per 5 ML Oral Solution

* Please review the disclaimer below.

Patient Education

Brompheniramine


Brompheniramine relieves red, irritated, itchy, watery eyes; sneezing; and runny nose caused by allergies, hay fever, and the common cold. Brompheniramine helps control symptoms, but does not treat the cause of the symptoms or speed recovery. Brompheniramine should not be used to cause sleepiness in children. Brompheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
[Learn More]


* 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".