basic care mucus dm

DEXTROMETHORPHAN HBR, GUAIFENESIN ORAL HUMAN OTC DRUG

basic care mucus dm is an FDA drug label for the active ingredient DEXTROMETHORPHAN HBR, GUAIFENESIN manufactured by Amazon.com 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 20210713.

Generic name
DEXTROMETHORPHAN HBR, GUAIFENESIN
Manufacturer
Amazon.com Services LLC
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
72288-812
Application
ANDA207602
Label effective
20210713

About this product

basic care mucus dm is an FDA-registered drug product whose active ingredient is DEXTROMETHORPHAN HBR, GUAIFENESIN. It is labelled by Amazon.com Services LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72288-812, application ANDA207602, label effective 20210713. It is one of 33 FDA drug label records sharing the active ingredient DEXTROMETHORPHAN HBR, GUAIFENESIN. 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 DEXTROMETHORPHAN HBR, GUAIFENESIN are most often described in connection with: helps loosen, phlegm mucus, thin bronchial, secretions rid, passageways bothersome, make coughs, productive temporarily, relieves cough. 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) Dextromethorphan HBr 60 mg Guaifenesin 1200 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: • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants • the intensity of coughing • the impulse to cough to help you get to sleep

Dosage & Administration

Directions • do not crush, chew, or break 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: 1 tablet every 12 hours; not more than 2 tablets in 24 hours • children under 12 years of age: do not use

Warnings

Warnings Do not use • for children under 12 years of age • 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 • 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 • cough lasts more than 7 days, comes back, or occurs with 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).

More products with the same ingredient

DEXTROMETHORPHAN HBR, GUAIFENESIN

7 Select Maximum Strength

7-ELEVEN View label

CVS Adult Cough plus Chest Congestion DM Max with Honey

CVS PHARMACY View label

CVS Maximum Strength

CVS PHARMACY View label

Chest Congestion Relief DM

DOLGENCORP, LLC View label

Cough and Chest Congestion DM

CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED View label

Cough and Chest Congestion DM Adult

CVS Pharmacy View label

DG health mucus dm

Dolgencorp, LLC View label

DM Max

Walgreen Company View label

How products containing DEXTROMETHORPHAN HBR, GUAIFENESIN compare

FDA lists 33 drug label records with DEXTROMETHORPHAN HBR, GUAIFENESIN 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
— — CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED 4
— — Akron Pharma Inc. 2
— — Amerisource Bergen 2
— — CVS PHARMACY 2
— — DOLGENCORP, LLC 2

Frequently asked questions

What is basic care mucus dm 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: • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants • the intensity of coughing • the impulse to cough to help you get to sleep

Who makes basic care mucus dm?
Amazon.com Services LLC is the labeler of record for basic care mucus dm. 33 FDA label records share the active ingredient DEXTROMETHORPHAN HBR, GUAIFENESIN, 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 basic care mucus dm 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 basic care mucus dm 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 DEXTROMETHORPHAN HBR, GUAIFENESIN?
Yes. 33 FDA drug label records list DEXTROMETHORPHAN HBR, GUAIFENESIN 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 basic care mucus dm 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.