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NDC 63868-0801-27 Mucus Relief D Sinus Congestion 400; 40 mg/1; mg/1 Details
Mucus Relief D Sinus Congestion 400; 40 mg/1; mg/1
Mucus Relief D Sinus Congestion is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by CHAIN DRUG MARKETING ASSOCIATION INC. The primary component is GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE.
MedlinePlus Drug Summary
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: 63868-0801-27Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.
Related Packages: 63868-0801-27Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pseudoephedrine
Product Information
| NDC | 63868-0801 |
|---|---|
| Product ID | 63868-801_6942d03c-6188-4f6e-bd39-392a47e26a66 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Mucus Relief D Sinus Congestion |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Guaifenesin, Pseudoephedrine HCl |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 400; 40 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Labeler Name | CHAIN DRUG MARKETING ASSOCIATION INC |
| Pharmaceutical Class | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M012 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63868-0801-27 (63868080127)
| NDC Package Code | 63868-801-27 |
|---|---|
| Billing NDC | 63868080127 |
| Package | 3 BLISTER PACK in 1 CARTON (63868-801-27) / 9 TABLET, FILM COATED in 1 BLISTER PACK |
| Marketing Start Date | 2020-04-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |