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  4. NDC Product Code: 53145-320 Defensol D (multi Symptom Effervescent Tablets)

NDC 53145-320 Defensol D (multi Symptom Effervescent Tablets)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53145-320?
  5. Defensol D (multi Symptom Effervescent Tablets) 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:
53145-320
Proprietary Name:
Defensol D (multi Symptom Effervescent Tablets)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Menper Distributors Inc.
Labeler Code:
53145
Product Label ID:
bb3b29d2-d705-48b9-8893-8a8ce4694bfb
Start Marketing Date: [9]
12-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
30 MM
Score:
1
Flavor(s):
ORANGE (C73406)

Product Packages

NDC Code 53145-320-06

Package Description: 6 POUCH in 1 BOX / 2 TABLET, EFFERVESCENT in 1 POUCH (53145-320-02)

Product Details

What is NDC 53145-320?

The NDC code 53145-320 is assigned by the FDA to the product Defensol D (multi Symptom Effervescent Tablets) which is product labeled by Menper Distributors Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53145-320-06 6 pouch in 1 box / 2 tablet, effervescent in 1 pouch (53145-320-02). 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 Defensol D (multi Symptom Effervescent Tablets)?

• Do not take more than the recommended dose• Adults and children 12 years and over: take 2 tablets fully dissolved in 4oz. of water every four hours. Do not exceed 8 tablets in 24 hours or as directed by a doctor• Children under 12 years: do not use

Which are Defensol D (multi Symptom Effervescent Tablets) UNII Codes?

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

Which are Defensol D (multi Symptom Effervescent Tablets) 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 Defensol D (multi Symptom Effervescent Tablets)?

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: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Effervescent Oral Tablet
  • RxCUI: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet
  • RxCUI: 1536477 - APAP 250 MG / Chlorpheniramine Maleate 2 MG / Dextromethorphan Hydrobromide 10 MG / Phenylephrine Hydrochloride 5 MG Effervescent Oral Tablet

* 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".