Active Ingredient(S)
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates, Llc for the product Mucus Relief Dm (NDC 76162-008). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use(s), do not use, ask a doctor before use if, ask a doctor or pharmacist before use if, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Cough suppressant
Expectorant
you are taking sedatives or tranquilizers
cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent
headache. These could be signs of a serious illness
ask a health professional before use.
In case of accidental overdose, get medical help or contact a Poison Control
Center (1-800-222-1222) right away.
Adults and children 12 years of age and older: Take 1 tablet every 4 hours with a
full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.
Children under 12 years of age: do not use
croscarmellose sodium, magnesium stearate, maltodextrin, microcrystalline cellulose,
povidone, silicon dioxide, stearic acid
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