Label: MUCOSA DM- dextromethorphan hydrobromide, guaifenesin tablet
- NDC Code(s): 54257-277-01
- Packager: Magno-Humphries, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 27, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- MHL NDC 54257-277-01 immediate Acting
- DO NOT USE IF PRINTED SEAL UNDER CAP IS MISSING OR DAMAGE
- Active ingredients (in each tablet)
- Purpose
- Uses
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Warnings
a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for two weeks after stopping the MAOI drug. If you do not know if your prescription drug contains MAOI, ask a doctor or pharmacist before taking this product. Do not use for children under 12. Do not use if you are now taking
cougha ccompanied with excessive phlegm (mucus), persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema. Ask a doctor before use if you have
do not use for more than 7 days. When using this product do not exceed recommended dosage
cough lasts for more than 7 days, recurs, or is accompanied with fever, rash, or persistent headache. These could be signs of a serious condition. Stop use and ask a doctor if
ask a health professional before use. If pregnant or breast-feeding,
- Directions
- Other information
- Inactive ingredients
- Questions?
- Distributed by: Magno-Humphries, Inc., OR 97223 U.S.A. Visit our website: www.magno-humphries.com
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
MUCOSA DM
dextromethorphan hydrobromide, guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54257-277 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 400 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score 2 pieces Shape OVAL Size 17mm Flavor Imprint Code AZ345 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54257-277-01 50 in 1 BOTTLE; Type 0: Not a Combination Product 04/04/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/04/2017 Labeler - Magno-Humphries, Inc. (063251433)