1. Home
  2. Labeler Index
  3. Mcr American Pharmaceuticals, Inc.
  4. NDC Product Code: 58605-306 Maxi-tuss Pe

NDC 58605-306 Maxi-tuss Pe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58605-306?
  5. Maxi-tuss Pe 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:
58605-306
Proprietary Name:
Maxi-tuss Pe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mcr American Pharmaceuticals, Inc.
Labeler Code:
58605
Product Label ID:
cd18a0d2-a5ff-4261-be1f-1d0e3774a06a
Start Marketing Date: [9]
08-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Flavor(s):
BUBBLE GUM (C73368)

Code Structure Chart

Product Details

What is NDC 58605-306?

The NDC code 58605-306 is assigned by the FDA to the product Maxi-tuss Pe 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 58605-306-16 473 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 Pe?

Do not exceed recommended dosage.Adults and children 12 years of age and over:2 teaspoonfuls every 4 hours, not to exceed 12 teaspoonfuls in 24 hours, or as directed by a doctor.Children 6 to under 12 years of age:1 teaspoonful every 4 hours, not to exceed 6 teaspoonfuls in 24 hours, or as directed by a doctor.Children under 6 years of age:consult a doctor

Which are Maxi-tuss Pe UNII Codes?

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

Which are Maxi-tuss Pe 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 Pe?

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: 1357013 - brompheniramine maleate 2 MG / phenylephrine HCl 5 MG per 5 mL Oral Syrup
  • RxCUI: 1357013 - brompheniramine maleate 0.4 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1357013 - brompheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG per 5 ML Oral Syrup

* 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]


Phenylephrine


Phenylephrine is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.
[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".