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NDC 70000-0565-01 Mucus Relief DM 20; 400 mg/20mL; mg/20mL Details
Mucus Relief DM 20; 400 mg/20mL; mg/20mL
Mucus Relief DM is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Cardinal Health (Leader) 70000. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.
MedlinePlus Drug Summary
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
Related Packages: 70000-0565-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Dextromethorphan
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
Related Packages: 70000-0565-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
NDC | 70000-0565 |
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Product ID | 70000-0565_3cf5c25c-bdbf-4f5e-ab05-e445d4c83c59 |
Associated GPIs | 43997002520905 |
GCN Sequence Number | 023893 |
GCN Sequence Number Description | guaifenesin/dextromethorphan LIQUID 100-5 MG/5 ORAL |
HIC3 | B3T |
HIC3 Description | NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION |
GCN | 53497 |
HICL Sequence Number | 000223 |
HICL Sequence Number Description | GUAIFENESIN/DEXTROMETHORPHAN HBR |
Brand/Generic | Generic |
Proprietary Name | Mucus Relief DM |
Proprietary Name Suffix | Maximum Strength |
Non-Proprietary Name | Dextromethorphan HBr, Guaifenesin |
Product Type | HUMAN OTC DRUG |
Dosage Form | LIQUID |
Route | ORAL |
Active Ingredient Strength | 20; 400 |
Active Ingredient Units | mg/20mL; mg/20mL |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Labeler Name | Cardinal Health (Leader) 70000 |
Pharmaceutical Class | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Ant |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 70000-0565-01 (70000056501)
NDC Package Code | 70000-0565-1 |
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Billing NDC | 70000056501 |
Package | 177 mL in 1 BOTTLE, PLASTIC (70000-0565-1) |
Marketing Start Date | 2020-04-30 |
NDC Exclude Flag | N |
Pricing Information | |
Price Per Unit | 0.01972 |
Pricing Unit | ML |
Effective Date | 2022-07-20 |
NDC Description | MUCUS RELIEF DM MAX LIQUID |
Pharmacy Type Indicator | C/I |
OTC | Y |
Explanation Code | 4, 5 |
Classification for Rate Setting | G |
As of Date | 2022-11-23 |
Standard Product Labeling (SPL)/Prescribing Information SPL c4971d15-c768-4370-b7b3-f0b4848e1758 Details
Uses
- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of botherosme 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
Warnings
Do not use
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 that occurs with too much phlegm (mucus)
Directions
- do not take more than 6 doses in any 24-hour period
- measure only with dosing cup provided. Do not use any other dosing device.
- keep dosing cup with product
- mL = milliliter
- dose as follows or as directed by a doctor
- adults and children 12 years of age and older: 20 mL every 4 hours
- children under 12 years of age: do not use
Other information
Inactive ingredients
Principal Display Panel
COMPARE TO MAXIMUM STRENGTH MUCINEX® FAST-MAX® DM MAX active ingredient
Maximum Strength Mucus Relief DM
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Cough Suppressant | Expectorant
For Ages 12 Years and Over
Controls Cough
Relieves Chest Congestion
Thin & Loosens Mucus 4 Hour Dosing
Questions or comments? Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
FL OZ (mL)
*This product is not manufactured or distributed by Reckitt Benckiser, distributor of Maximum Strength Mucinex® Fast-Max® DM Max.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY CARDINAL HEALTH
DUBLIN, OHIO 43017
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM
MAXIMUM STRENGTH
dextromethorphan hbr, guaifenesin liquid |
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Labeler - Cardinal Health (Leader) 70000 (063997360) |