Home NDC 83324-024-04 QCH Adult Tussin 541
Product NDC 83324-024
Requested package NDC 83324-024-04
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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base QCH Adult Tussin 541
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 200 mg/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 495W7451VQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 310604 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83324-024-04 QCH Adult Tussin 541 1 in 1 CARTON LIQUID 1 1 83324-024-04 QCH Adult Tussin 541 118 mL in 1 BOTTLE LIQUID 118 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83324-024 QCH ADULT TUSSIN 541 (GUAIFENESIN) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC.] 1 Current NDC, 2 package rows 20240504_b487f4af-ad0c-4f18-9a6b-7fd386b3f46c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83324-024-04 83324002404 1 BOTTLE in 1 CARTON (83324-024-04) / 118 mL in 1 BOTTLE 1 bottle 2024-05-02 No No Current