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  4. NDC Product Code: 58605-305 Maxi-tuss Tr

NDC 58605-305 Maxi-tuss Tr

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58605-305?
  5. Maxi-tuss Tr 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:
58605-305
Proprietary Name:
Maxi-tuss Tr
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mcr American Pharmaceuticals, Inc.
Labeler Code:
58605
Product Label ID:
132fff99-f8fa-4cc5-9cd1-c39a048511b5
Start Marketing Date: [9]
08-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
BUBBLE GUM (C73368)

Product Packages

NDC Code 58605-305-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 58605-305?

The NDC code 58605-305 is assigned by the FDA to the product Maxi-tuss Tr which is product labeled by Mcr American Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58605-305-16 473 ml in 1 bottle, plastic . 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 Maxi-tuss Tr?

Do not exceed recommended dosage.Adults and children 12 years of age and over:2 teaspoonfuls (10 mL) every 4-6 hours, not to exceed 8 teaspoonfuls in 24 hoursChildren 6 to under 12 years of age:1 teaspoonful (5 mL) every 4-6 hours, not to exceed 4 teaspoonfuls in 24 hoursChildren under 6 years of age:Consult a physician

Which are Maxi-tuss Tr UNII Codes?

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

Which are Maxi-tuss Tr 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 Maxi-tuss Tr?

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: 1099308 - pseudoephedrine HCl 30 MG / triprolidine HCl 1.25 MG in 5 mL Oral Solution
  • RxCUI: 1099308 - pseudoephedrine hydrochloride 6 MG/ML / triprolidine hydrochloride 0.25 MG/ML Oral Solution
  • RxCUI: 1099308 - pseudoephedrine hydrochloride 30 MG / triprolidine hydrochloride 1.25 MG per 5 ML Oral Solution

* 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".