Mucus Relief Extended Release Maximum Strength

GUAIFENESIN ORAL HUMAN OTC DRUG

Mucus Relief Extended Release Maximum Strength is an FDA drug label for the active ingredient GUAIFENESIN manufactured by H E B 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 20221209.

Generic name
GUAIFENESIN
Manufacturer
H E B
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
37808-762
Application
ANDA207342
Label effective
20221209

Active ingredients

Active ingredient (in each extended-release tablet) Guaifenesin 1200 mg

Indications & Usage

Uses Helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and makes coughs more productive.

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 the timing of meals adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours. children under 12 years of age: do not use

Contraindications

Not available.

Warnings

Warnings Do not use for children under 12 years of age. 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) 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).

Adverse Reactions

Not available.

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