Home NDC 46122-794 Mucus Relief
Product NDC 46122-794
11-digit product format 461220794
Labeler code 46122
Product ID 46122-794_e85ab29d-ff4c-4781-8446-35399605ac8d
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Amerisource Bergen
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-08
Substance GUAIFENESIN
Active strength 400 mg/1
Pharmacologic classes Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 Mucus Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 400 mg/1
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 359601 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 46122-794-61 Mucus Relief 50 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 50 5 46122-794-61 Mucus Relief 1 in 1 CARTON TABLET, FILM COATED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46122-794 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [AMERISOURCE BERGEN] 4 Current NDC, 2 package rows 20250323_087a3a0b-8d3f-45ed-8807-0af47b446cac.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 73 of 178 · 3,551 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 46122-794-61 46122079461 1 BOTTLE, PLASTIC in 1 CARTON (46122-794-61) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2024-08-08 No No Current