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Drug Facts
Dist. by: RB Health (US)
Parsippany, NJ 07054-0224
Made in England
The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Mucinex Dm (NDC 50090-6549). 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 other, otc - purpose, uses, do not use, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, otc - pregnancy or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Dist. by: RB Health (US)
Parsippany, NJ 07054-0224
Made in England
| Active ingredients (in each extended-release bi-layer tablet) | Purposes |
|---|---|
| Dextromethorphan HBr 60 mg | Cough suppressant |
| Guaifenesin 1200 mg | Expectorant |
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.
carbomer homopolymer type B; D&C yellow no. 10 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF
1-866-MUCINEX (1-866-682-4639) You may also report side effects to this phone number.
Product: 50090-6549
NDC: 50090-6549-0 14 TABLET, EXTENDED RELEASE in a BLISTER PACK / 24 in a CARTON
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