NDC 23558-5504 Cheracol D Cough Formula 4oz

NDC Product Code 23558-5504

NDC CODE: 23558-5504

Proprietary Name: Cheracol D Cough Formula 4oz What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 23558-5504-0

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 118 mL in 1 BOTTLE, PLASTIC (23558-5504-1)

NDC 23558-5504-2

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 177 mL in 1 BOTTLE, PLASTIC (23558-5504-3)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Cheracol D Cough Formula 4oz with NDC 23558-5504 is a product labeled by Lee Pharmaceuticals. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 996520.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • FRUCTOSE (UNII: 6YSS42VSEV)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SUCROSE (UNII: C151H8M554)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Lee Pharmaceuticals
Labeler Code: 23558
Start Marketing Date: 12-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Information for Patients

Dextromethorphan

Dextromethorphan is pronounced as (dex troe meth or' fan)

Why is dextromethorphan medication prescribed?
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat th...
[Read More]
Guaifenesin

Guaifenesin is pronounced as (gwye fen' e sin)
Why is guaifenesin medication prescribed?
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a cla...
[Read More]

* Please review the disclaimer below.

Cheracol D Cough Formula 4oz Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients (5 Ml Teaspoonful)

Dextromethorphan HBr, 10mgGuaifenesin, 100mg

Purpose

Cough suppressantExpectorant

Uses

  • Temporarily quiets coughs due to minor throat and bronchial irritation associated with the common cold.Helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes.

Warnings

  • Do not useif you are now taking a perscription monoamine oxidase inhibitor (MAOI) ( certain drugs for depression, psychiatric or emotional conditions or Parkinson's disease) or for 2 weeks after stopping the MAOI drug.  If you're uncertain whether your prescription drug contains MAOI, ask a doctor or pharmacist before taking this product.

Ask A Doctor Before Use If You Have

  • A persistent chronic cough such as occurs with smoking, asthma or emphysema.excessive phlegm (mucus).

Stop Use And Ask A Doctor If

  • Cough persists for more than one weekcough tends to recur or is accompanied by fever, rash or persistent headache.  A persistent cough may be a sign of a serious condition.

Directions

  • Follow dosage below or use as directed by a doctorDo not exceed 6 dosages in 24 hoursAdults and children 12 years or age and over, 2 teaspoonfuls every 4 hoursChildren 6 to under 12 years of age, 1 teaspoonful every 4 hoursChildren under 6 years of age, consult a doctor

Other Information

Store from 15° - 30°C (59° - 86°F)

Inactive Ingredients

Alcohol 4.75%, benzoic acid, FD&C red #40, flavors, fructose, glycerin, propylene glycol, sodium chloride, sucrose, water.

* Please review the disclaimer below.