QCH Adult Tussin 541

Product NDC
83324-024
11-digit product format
833240024
Labeler code
83324
Product ID
83324-024_b487f4af-ad0c-4f18-9a6b-7fd386b3f46c
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
Chain Drug Marketing Association Inc.
Application
part341
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-05-02
Substance
GUAIFENESIN
Active strength
200 mg/10mL
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
495W7451VQGUAIFENESIN93-14-1GUAIFENESIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83324-024-04833240024041 BOTTLE in 1 CARTON (83324-024-04) / 118 mL in 1 BOTTLE1 bottle2024-05-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
QCH Adult Tussin 541Chain Drug Marketing Association Inc. | Guardian Drug Company2024-05-02Human OTC Drug Label1