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Curatussin - Medication Information

Product NDC Code 83335-101
Drug Name

Curatussin

Type Brand
Pharm Class Decreased Respiratory Secretion Viscosity [PE],
Expectorant [EPC],
Increased Respiratory Secretions [PE]
Active Ingredients
Guaifenesin 100 mg/5ml
Route ORAL
Dosage Form SOLUTION
RxCUI drug identifier 310604
Application Number M012
Labeler Name Wittman Pharma, Inc.
Packages
Package NDC Code Description
83335-101-04 118 ml in 1 bottle, plastic (83335-101-04)
83335-101-08 237 ml in 1 bottle, plastic (83335-101-08)
83335-101-16 473 ml in 1 bottle, plastic (83335-101-16)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient (in each 5 mL tsp) Guaifenesin 100 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Dosage & Admin Directions: ■ do not take more than 6 doses in any 24-hour period. AGE DOSE Adults & Children 12 years and over 2-4 teaspoonfuls every 4 hours Children 6 years to under 12 years 1-2 teaspoonfuls every 4 hours Children 2 to under 6 years 1/2 - 1 teaspoonfuls every 4 hours Children Under 2 years Ask a Doctor
AGEDOSE
Adults & Children 12 years and over2-4 teaspoonfuls every 4 hours
Children 6 years to under 12 years1-2 teaspoonfuls every 4 hours
Children 2 to under 6 years1/2 - 1 teaspoonfuls every 4 hours
Children Under 2 yearsAsk a Doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Citric Acid, Flavor, Methylparaben, Monoammonium Glycyrrhizinate, Potassium Citrate, Propylene Glycol, Propylparaben, Purified Water, Sorbitol, Sucralose

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses: ■ helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Purpose

Information about the drug product’s indications for use.
Purpose: Expectorant

Spl product data elements

Usually a list of ingredients in a drug product.
CuraTUSSIN Guaifenesin GUAIFENESIN GUAIFENESIN PROPYLENE GLYCOL SUCRALOSE PROPYLPARABEN POTASSIUM CITRATE METHYLPARABEN ANHYDROUS CITRIC ACID AMMONIUM GLYCYRRHIZATE SORBITOL WATER

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
CuraTUSSIN Label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Warnings: Ask a doctor before use if you have ■ cough that occurs with too much phlegm (mucus) ■ cough that lasts or is chronic, such as occurs with smoking, asthma, Chronic bronchitis, or emphysema 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. If pregnant of 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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API