NDC 53807-531 Cough Formula Cough And Cold

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53807-531
Proprietary Name:
Cough Formula Cough And Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rij Pharmaceutical Corporation
Labeler Code:
53807
Start Marketing Date: [9]
03-16-1999
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 53807-531-04

Package Description: 118 mL in 1 BOTTLE

NDC Code 53807-531-08

Package Description: 236 mL in 1 BOTTLE

Product Details

What is NDC 53807-531?

The NDC code 53807-531 is assigned by the FDA to the product Cough Formula Cough And Cold which is product labeled by Rij Pharmaceutical Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 53807-531-04 118 ml in 1 bottle , 53807-531-08 236 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 Cough Formula Cough And Cold?

Do not take more than 6 doses in any 24-hour periodagedoseadults and children 12 years and over2 teaspoonfuls every 4 hourschildren 6 years to under 12 years1 teaspoonful every 4 hourschildren 2 years to under 6 years1/2 teaspoonful every 4 hourschildren under 2 yearsask a doctor

Which are Cough Formula Cough And Cold UNII Codes?

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

Which are Cough Formula Cough And Cold 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 Cough Formula Cough And Cold?

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: 1044949 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral Solution
  • RxCUI: 1044949 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 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".