Country: United States
Language: English
Source: NLM (National Library of Medicine)
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)
McKesson
GUAIFENESIN
GUAIFENESIN 600 mg
OTC DRUG
Abbreviated New Drug Application
SUNMARK MUCUS ER- GUAIFENESIN TABLET, EXTENDED RELEASE MCKES S ON ---------- MCKESSON MUCUS•ER DRUG FACTS ACTIVE INGREDIENT (IN EACH EXTENDED-RELEASE TABLET) Guaifenesin 600 mg PURPOS E Expectorant US ES helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive WARNINGS DO NOT USE • ASK A DOCTOR BEFORE USE IF YOU HAVE • • STOP USE AND ASK A DOCTOR IF • 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) DIRECTIONS • • • • • for children under 12 years of age persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus) cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness. 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: one or two tablets every 12 hours. Do not exceed 4 tablets in 24 hours. children under 12 years of age: do not use OTHER INFORMATION • • INACTIVE INGREDIENTS compressible sugar, copovidone, hydroxyethyl cellulose, silicon dioxide, zinc stearate QUESTIONS OR COMMENTS? 1-800-719-9260 PACKAGE/LABEL PRINCIPAL DISPLAY PANEL COMPARE TO MUCINEX® ACTIVE INGREDIENT mucus•ER Guaifenesin Extended-Release Tablets, 600 mg Expectorant Relieves chest congestion Thins & loosens mucus 12 HOUR ACTUAL SIZE GLUTEN FREE 40 EXTENDED-RELEASE TABLETS do not use if printed seal under cap is broken or missing store between 20-25°C (68-77°F) SUNMARK MUCUS ER guaifenesin tablet, extended release PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:49 348 -9 0 5 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRE Read the complete document