foster and thrive adult tussin dm

Product NDC
70677-1035
11-digit product format
706771035
Labeler code
70677
Product ID
70677-1035_8f04e7be-88f6-4ece-b1db-3f17fa1ac312
Type
HUMAN OTC DRUG
Nonproprietary name
dextromethorphan hydrobromide, guaifenesin
Dosage form
SOLUTION
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-10-25
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20; 200 mg/20mL; mg/20mL
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 formatDescriptionUnitsMarketing startSampleExclude flagStatus
70677-1035-1706771035011 BOTTLE in 1 CARTON (70677-1035-1) / 118 mL in 1 BOTTLE1 bottle2023-10-25NoNoHistorical
70677-1035-2706771035021 BOTTLE in 1 CARTON (70677-1035-2) / 237 mL in 1 BOTTLE1 bottle2023-10-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
McKesson Adult Tussin DM Drug FactsStrategic Sourcing Services LLC2024-11-10HUMAN OTC DRUG LABEL2