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NDC 63739-0506-10 GUAIFENESIN DM 20; 200 mg/10mL; mg/10mL Details
GUAIFENESIN DM 20; 200 mg/10mL; mg/10mL
GUAIFENESIN DM is a ORAL SYRUP in the HUMAN OTC DRUG category. It is labeled and distributed by McKesson Corporation dba SKY Packaging. The primary component is DEXTROMETHORPHAN; 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: 63739-0506-10Last Updated: 04/28/2024
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: 63739-0506-10Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 63739-0506 |
|---|---|
| Product ID | 63739-506_357e51c7-84d4-40c9-8a69-db81f3ebc697 |
| Associated GPIs | |
| GCN Sequence Number | 016414 |
| GCN Sequence Number Description | guaifenesin/dextromethorphan SYRUP 100-10MG/5 ORAL |
| HIC3 | B3T |
| HIC3 Description | NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION |
| GCN | 53495 |
| HICL Sequence Number | 000223 |
| HICL Sequence Number Description | GUAIFENESIN/DEXTROMETHORPHAN HBR |
| Brand/Generic | Generic |
| Proprietary Name | GUAIFENESIN DM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | GUAIFENESIN and DEXTROMETHORPHAN |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SYRUP |
| Route | ORAL |
| Active Ingredient Strength | 20; 200 |
| Active Ingredient Units | mg/10mL; mg/10mL |
| Substance Name | DEXTROMETHORPHAN; GUAIFENESIN |
| Labeler Name | McKesson Corporation dba SKY Packaging |
| 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 DRUG |
| Application Number | M012 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 63739-0506-10 (63739050610)
| NDC Package Code | 63739-506-10 |
|---|---|
| Billing NDC | 63739050610 |
| Package | 10 TRAY in 1 CASE (63739-506-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (63739-506-01) |
| Marketing Start Date | 2024-01-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |