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NDC 41163-0813-34 equaline adult tussin 20; 200 mg/20mL; mg/20mL Details
equaline adult tussin 20; 200 mg/20mL; mg/20mL
equaline adult tussin is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by United Natural Foods, Inc. dba UNFI. 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: 41163-0813-34Last 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: 41163-0813-34Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
NDC | 41163-0813 |
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Product ID | 41163-813_6f0523c8-2188-4ce4-b788-4dc7679583db |
Associated GPIs | |
GCN Sequence Number | 079414 |
GCN Sequence Number Description | guaifenesin/dextromethorphan LIQUID 50-5MG/5ML ORAL |
HIC3 | B3T |
HIC3 Description | NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION |
GCN | 45903 |
HICL Sequence Number | 000223 |
HICL Sequence Number Description | GUAIFENESIN/DEXTROMETHORPHAN HBR |
Brand/Generic | Generic |
Proprietary Name | equaline adult tussin |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | dextromethorphan hydrobromide, guaifenesin |
Product Type | HUMAN OTC DRUG |
Dosage Form | SOLUTION |
Route | ORAL |
Active Ingredient Strength | 20; 200 |
Active Ingredient Units | mg/20mL; mg/20mL |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Labeler Name | United Natural Foods, Inc. dba UNFI |
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 41163-0813-34 (41163081334)
NDC Package Code | 41163-813-34 |
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Billing NDC | 41163081334 |
Package | 1 BOTTLE in 1 CARTON (41163-813-34) / 237 mL in 1 BOTTLE |
Marketing Start Date | 2022-06-08 |
NDC Exclude Flag | N |
Pricing Information | N/A |