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NDC 00363-7470-04 Walgreens 20; 200 mg/20mL; mg/20mL Details
Walgreens 20; 200 mg/20mL; mg/20mL
Walgreens is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by WALGREENS. 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: 00363-7470-04Last Updated: 11/30/2022
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: 00363-7470-04Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
NDC | 00363-7470 |
---|---|
Product ID | 0363-7470_788327a0-723c-4b80-b281-5873de0b6905 |
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 | Walgreens |
Proprietary Name Suffix | Grape Flavor |
Non-Proprietary Name | Children Cough and Chest Congestion |
Product Type | HUMAN OTC DRUG |
Dosage Form | LIQUID |
Route | ORAL |
Active Ingredient Strength | 20; 200 |
Active Ingredient Units | mg/20mL; mg/20mL |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Labeler Name | WALGREENS |
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 | 2024-12-31 |
Package
NDC 00363-7470-04 (00363747004)
NDC Package Code | 0363-7470-04 |
---|---|
Billing NDC | 00363747004 |
Package | 1 BOTTLE in 1 CARTON (0363-7470-04) / 118 mL in 1 BOTTLE |
Marketing Start Date | 2019-05-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |