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  4. NDC Product Code: 58238-226 Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor

NDC 58238-226 Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58238-226?
  5. Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
58238-226
Proprietary Name:
Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Deliz Pharmaceutical Corp
Labeler Code:
58238
Product Label ID:
93e0411b-68c2-4b5c-aa74-b1d94b5b2206
Start Marketing Date: [9]
03-20-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - CHERRY FLAVOR)

Product Packages

NDC Code 58238-226-04

Package Description: 1 BOTTLE in 1 PACKAGE / 118 mL in 1 BOTTLE

Product Details

What is NDC 58238-226?

The NDC code 58238-226 is assigned by the FDA to the product Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor which is product labeled by Deliz Pharmaceutical Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58238-226-04 1 bottle in 1 package / 118 ml in 1 bottle. 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 Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor?

Use only with enclosed measuring cupdo not use enclosed measuring cup for any other drug product Adults and children 12 years of age and older: 2 teaspoonfuls (tsp) every 6 hours not to exceed 8 teaspoonfuls in 24 hours, or as directed by a doctor. Children 6 to under 12 years of age: 1 teaspoonful (tsp) every 6 hours not to exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor. Children 2 to under 6 years of age: Consult a doctor.

Which are Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor UNII Codes?

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

  • DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW)
  • DEXCHLORPHENIRAMINE (UNII: 3Q9Q0B929N) (Active Moiety)
  • PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
  • PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)

Which are Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor 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 Deltuss Dp Nasal Decongestant Antihistamine Cherry Flavor?

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: 1298226 - dexchlorpheniramine maleate 1 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1298226 - dexchlorpheniramine maleate 0.2 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1298226 - dexchlorpheniramine maleate 1 MG / pseudoephedrine HCl 30 MG per 5 ML Oral Solution

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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".