NDC 0113-0958 Good Sense Cough Dm

Dextromethorphan Polistirex

NDC Product Code 0113-0958

NDC 0113-0958-21

Package Description: 1 BOTTLE in 1 CARTON > 89 mL in 1 BOTTLE

NDC 0113-0958-28

Package Description: 1 BOTTLE in 1 CARTON > 148 mL in 1 BOTTLE

NDC Product Information

Good Sense Cough Dm with NDC 0113-0958 is a a human over the counter drug product labeled by L. Perrigo Company. The generic name of Good Sense Cough Dm is dextromethorphan polistirex. The product's dosage form is suspension and is administered via oral form.

Labeler Name: L. Perrigo Company

Dosage Form: Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Good Sense Cough Dm Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • DEXTROMETHORPHAN HYDROBROMIDE 30 mg/5mL

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • POVIDONES (UNII: FZ989GH94E)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM METABISULFITE (UNII: 4VON5FNS3C)
  • SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
  • SUCROSE (UNII: C151H8M554)
  • TARTARIC ACID (UNII: W4888I119H)
  • TRAGACANTH (UNII: 2944357O2O)
  • TRIACETIN (UNII: XHX3C3X673)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • POLYVINYL ACETATE (UNII: 32K497ZK2U)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: L. Perrigo Company
Labeler Code: 0113
FDA Application Number: ANDA091135 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-20-2013 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: 12-31-2021 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: N 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. Values = ‘Y’ or ‘N’.

* 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]

* Please review the disclaimer below.

Good Sense Cough Dm Product Label Images

Good Sense Cough 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

Active Ingredient (In Each 5 Ml)

Dextromethorphan polistirex equivalent to 30 mg dextromethorphan hydrobromide

Purpose

Cough suppressant

Uses

  • Temporarily relieves •cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants •the impulse to cough to help you get to sleep

Do Not Use

If you are now taking a prescription 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 do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.Allergy Alert: Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions.

Ask A Doctor Before Use If You Have

  • •chronic cough that lasts as occurs with smoking, asthma or emphysema •cough that occurs with too much phlegm (mucus)

Stop Use And Ask A Doctor If

  • •side effects occur. You may report side effects to FDA at 1-800-FDA-1088. •cough lasts more than 7 days, cough comes back, or occurs with fever, rash or headache that lasts. These could be signs of a serious condition.

If Pregnant Or Breast-Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

In case of overdose, get medical help or contact a Poison Control Center right away 1-800-222-1222.

Directions

  • •shake bottle well before use •measure only with dosing cup provided. Do not use dosing cup with other products. •dose as follows or as directed by doctor •mL = milliliteradults and children12 years of age and over10 mL every 12 hours,not to exceed 20 mL in 24 hourschildren 6 to under12 years of age5 mL every 12 hours,not to exceed 10 mL in 24 hourschildren 4 to under6 years of age2.5 mL every 12 hours,not to exceed 5 mL in 24 hourschildren under 4 years of agedo not use

Other Information

  • •each 5 mL contains: sodium 5 mg •store at 20° to 25°C (68° to 77°F) •dosing cup provided

Inactive Ingredients

D&C Red #30 aluminum lake, D&C Yellow #10 aluminum lake, flavor, glycerin, high fructose corn syrup, methylparaben, polysorbate 80, polyvinyl acetate, povidone, propylparaben, purified water, sodium metabisulfite, sodium polystyrene sulfonate, sucrose, tartaric acid, tragacanth gum, triacetin, xanthan gum

* Please review the disclaimer below.