Search by Drug Name or NDC
NDC 70000-0129-01 Maximum Strength Mucus Relief DM 20; 400 mg/20mL; mg/20mL Details
Maximum Strength Mucus Relief DM 20; 400 mg/20mL; mg/20mL
Maximum Strength Mucus Relief DM is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by CARDINAL HEALTH. 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: 70000-0129-01Last 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: 70000-0129-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 70000-0129 |
|---|---|
| Product ID | 70000-0129_c732d183-f208-4fc8-b41f-d8856298cf51 |
| 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 | Maximum Strength Mucus Relief DM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Dextromethorphan hydrobromide and Guaifenesin |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 20; 400 |
| Active Ingredient Units | mg/20mL; mg/20mL |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Labeler Name | CARDINAL HEALTH |
| 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
NDC 70000-0129-01 (70000012901)
| NDC Package Code | 70000-0129-1 |
|---|---|
| Billing NDC | 70000012901 |
| Package | 180 mL in 1 BOTTLE (70000-0129-1) |
| Marketing Start Date | 2017-03-06 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.0185 |
| Pricing Unit | ML |
| Effective Date | 2024-01-17 |
| 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 | 2024-02-21 |