Tussin DM Cough and Chest Congestion

Product NDC
21130-583
11-digit product format
211300583
Labeler code
21130
Product ID
21130-583_e3534cc1-edf9-482f-8462-8d08d36790f3
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan HBr, Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
Safeway, Inc.
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-01
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20; 200 mg/10mL; mg/10mL
Pharmacologic classes
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 Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
9D2RTI9KYHDEXTROMETHORPHAN HYDROBROMIDE6700-34-1DEXTROMETHORPHAN HYDROBROMIDE
495W7451VQGUAIFENESIN93-14-1GUAIFENESIN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
21130-583-04211300583041 BOTTLE, PLASTIC in 1 BOX (21130-583-04) / 118 mL in 1 BOTTLE, PLASTIC2025-12-01NoNoHistorical
21130-583-08211300583081 BOTTLE, PLASTIC in 1 BOX (21130-583-08) / 237 mL in 1 BOTTLE, PLASTIC2025-12-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsSafeway, Inc.2025-11-05HUMAN OTC DRUG LABEL1