Label: MUCUS RELIEF DM- guaifenesin, dextromethorphan hbr tablet, extended release
- NDC Code(s): 37808-733-40
- Packager: H E B
- This is a repackaged label.
- Source NDC Code(s): 65162-038
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 22, 2023
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- Official Label (Printer Friendly)
- Active ingredients (in each extended-release tablet)
- Purpose
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Uses
- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
- temporarily relieves
- cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
- the intensity of coughing
- the impulse to cough to help you get to sleep
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Warnings
Do not use
- for children under12 years of age
- if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
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)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to Mucinex® DM active ingredients*
Mucus Relief DM
Extended Release
Guaifenesin, 600 mg / Expectorant
Dextromethorphan HBr, 30 mg / Cough Suppressant
Expectorant / Cough Suppressant
- Controls cough
- Thins & loosen mucus
EXTENDED-RELEASE TABLETS
*This product is not manufactured or distributed Reckitt Benckiser LLC, distributor of Mucinex® DM.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
MADE WITH PRIDE AND CARE
FOR H-E-B®
SAN ANTONIO, TX 78204
- Package Label
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM
guaifenesin, dextromethorphan hbr tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-733(NDC:65162-038) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) CARBOMER 934 (UNII: Z135WT9208) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color yellow (light yellow) Score no score Shape OVAL Size 16mm Flavor Imprint Code AN038 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-733-40 1 in 1 BOX 02/28/2023 1 40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA209692 02/28/2023 Labeler - H E B (007924756)