foster and thrive mucus relief d

GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE ORAL HUMAN OTC DRUG

foster and thrive mucus relief d is an FDA drug label for the active ingredient GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE manufactured by Strategic Sourcing Services LLC administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260804.

Generic name
GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Manufacturer
Strategic Sourcing Services LLC
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
70677-1272
Application
ANDA214407
Label effective
20260804

About this product

foster and thrive mucus relief d is an FDA-registered drug product whose active ingredient is GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE. It is labelled by Strategic Sourcing Services LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 70677-1272, application ANDA214407, label effective 20260804. It is one of 10 FDA drug label records sharing the active ingredient GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, helps loosen, phlegm mucus, thin bronchial, secretions rid, passageways bothersome, make coughs, nasal congestion. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients (in each extended-release tablet) Guaifenesin 600 mg Pseudoephedrine HCl 60 mg

Indications & Usage

Uses • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive • temporarily relieves nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily restores freer breathing through the nose • promotes nasal and/or sinus drainage • temporarily relieves sinus congestion and pressure

Dosage & Administration

Directions • do not crush, chew, or break extended-release tablet • take with a full glass of water • this product can be administered without regard for timing of meals • adults and children 12 years and older: 2 extended-release tablets every 12 hours; not more than 4 extended-release tablets in 24 hours • children under 12 years of age: do not use

Warnings

Warnings 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. Ask a doctor before use if you have • heart disease • high blood pressure • thyroid disease • diabetes • trouble urinating due to an enlarged prostate gland • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema • cough accompanied by too much phlegm (mucus) When using this product • do not use more than directed Stop use and ask a doctor if • you get nervous, dizzy, or sleepless • symptoms do not get better within 7 days, come back or occur with a fever, rash, or persistent headache. These could be signs of a serious illness. 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).

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GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE

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How products containing GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE compare

FDA lists 10 drug label records with GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Reckitt Benckiser LLC 2
— — CVS Pharmacy 1
— — CVS Pharmacy, Inc. 1
— — PUBLIX SUPER MARKETS, INC 1
— — RUGBY LABORATORIES, INC. 1

Frequently asked questions

What is foster and thrive mucus relief d used for?
Uses • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive • temporarily relieves nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily restores freer breathing through the nose • promotes nasal and/or sinus drainage • temporarily relieves sinus congestion and …

Who makes foster and thrive mucus relief d?
Strategic Sourcing Services LLC is the labeler of record for foster and thrive mucus relief d. 10 FDA label records share the active ingredient GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does foster and thrive mucus relief d come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is foster and thrive mucus relief d prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE?
Yes. 10 FDA drug label records list GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has foster and thrive mucus relief d been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.