NDC 10956-674 Double Tussin Intense Cough Reliever DM

NDC Product Code 10956-674

NDC CODE: 10956-674

Proprietary Name: Double Tussin Intense Cough Reliever DM 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.

Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

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

NDC Code Structure

NDC 10956-674-01

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 120 mL in 1 BOTTLE, PLASTIC (10956-674-04)

NDC 10956-674-08

Package Description: 240 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Double Tussin Intense Cough Reliever DM with NDC 10956-674 is a product labeled by Reese Pharmaceutical Co. The generic name of Double Tussin Intense Cough Reliever DM is . The product's dosage form is and is administered via form.

Labeler Name: Reese Pharmaceutical Co

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.

  • POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • SORBITOL (UNII: 506T60A25R)

Product Labeler Information

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

Labeler Name: Reese Pharmaceutical Co
Labeler Code: 10956
Start Marketing Date: 08-02-2011 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: 12-31-2018 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...
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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.

Double Tussin Intense Cough Reliever DM Product Label Images

Double Tussin Intense Cough Reliever DM 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

Otc - Active Ingredient

Active ingredient per 5ml teaspoonDextromethorphan Hydrobromide   20mg   Cough SuppressantGuaifenesin  300mg  Expectorant

Indications & Usage

Uses. temporarily relieves cough due to minor throat and bronchial irritation as may occur with a common cold • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus • helps make coughs more productive

Warnings

Do not use if you are now taking a prescription monoamine oxidase (inhiMor~MAIO)Certain drugs for depression, psychiatric or emotional conditioners or Parkinson's diseaseor for 2 weeks after stopping MAIO drug, If you do not know if your prescription drug containsan MAIO, ask your doctor or pharmacist before using this product

Otc - Ask Doctor

Ask doctor before use if you havepersistent or chronic cough, such as occurs with smoking, asthma, bronchitis or emphysmacough is accompanied by excessive phlegm (mucous)

Otc - Stop Use

Stop use and ask doctor ifSymptoms are accompanied by fever, rash or persistent headachecough persists for more than 1 week or tends to recurA persistent cough may be a sign of a serious condition

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use

Otc - Keep Out Of Reach Of Children

Keep out of reach of children, In  case of overdose, get medical help or contact a Poison Center immediately

Dosage & Administration

Directions         • Adults and children 12 years of age and over:     take 1 tablet every 4 hours as needed     • Children 6 to 10 under 12 years of age: take 1/2 tablet every 4 hours as needed • Children under 6 years of age: consult a doctor     Do not exceed 6 doses in a 24 hour period or as directed by a doctor Other information store at 15'- 30' C (59'- 86'F)

Otc - Purpose

PurposeDextromethorphan Hydrobromide      Cough SuppressantGuaifenesin                                     Expectorant

Inactive Ingredient

Cherry Flavor,Citric Acid,Menthol,Polyethylene Glycol,Propylene Glycol,Purified Water,Sodium Benzoate,Sodium Saccharin,Sorbitol.

* Please review the disclaimer below.