NDC 0031-8724 Robitussin Mucus Plus Chest Congestion

NDC Product Code 0031-8724

NDC 0031-8724-12

Package Description: 1 BOTTLE in 1 CARTON > 118 mL in 1 BOTTLE

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

NDC Product Information

Robitussin Mucus Plus Chest Congestion with NDC 0031-8724 is a product labeled by Richmond Division Of Wyeth. The generic name of Robitussin Mucus Plus Chest Congestion is . The product's dosage form is and is administered via form.

Labeler Name: Richmond Division Of Wyeth

Dosage Form: -

Product Type: 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.

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.

  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • CARAMEL (UNII: T9D99G2B1R)
  • DEXTROSE (UNII: IY9XDZ35W2)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • PROPYLENE GLYCOL, (R)- (UNII: 602HN5L69H)
  • SACCHARIN SODIUM (UNII: SB8ZUX40TY)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)

Product Labeler Information

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

Labeler Name: Richmond Division Of Wyeth
Labeler Code: 0031
Start Marketing Date: 07-18-2012 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: 12-31-2019 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 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

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.

Robitussin Mucus Plus Chest Congestion 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

Other

Drug Facts

Distributed by:Pfizer, Madison, NJ 07940 USAFor most recent product information, visit www.robitussin.com

Active Ingredient (In Each 10 Ml)

Guaifenesin, USP 200 mg

Purpose

Expectorant

Use

Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Otc - Ask Doctor

  • Ask a doctor before use if you havecough that occurs with too much phlegm (mucus)cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Otc - Stop Use

Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, 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 Control Center right away.

Directions

  • Do not take more than 6 doses in any 24-hour periodmeasure only with dosing cup providedkeep dosing cup with productml=milliliterthis adult product is not intended for use in children under 12 years of ageagedoseadults and children 12 years and over10-20 ml every 4 hourschildren under 12 yearsdo not use

Other Information

  • Each 10 ml contains: sodium 4 mgstore at 20-25°C (68-77°F). Do not refrigeratealcohol-free

Inactive Ingredients

Anhydrous citric acid, artificial flavor, caramel, FD&C red no. 40, glycerin, high fructose corn syrup, liquid glucose, menthol, propylene glycol, purified water, saccharin sodium, sodium benzoate

* Please review the disclaimer below.