Home NDC 71679-119 Mucus Relief
Product NDC 71679-119
11-digit product format 716790119
Labeler code 71679
Product ID 71679-119_55feab68-a22d-b260-e063-6294a90ad86a
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin 400 mg
Dosage form TABLET
Route ORAL
Labeler Health Pharma USA LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-18
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 71679-119-02 Mucus Relief 200 in 1 BOTTLE TABLET 200 11 71679-119-60 Mucus Relief 60 in 1 BOTTLE TABLET 60 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71679-119 MUCUS RELIEF (GUAIFENESIN 400 MG) TABLET [HEALTH PHARMA USA LLC] 3 Current NDC, Legacy NDC, 2 package rows 20231031_d60a3e9d-e88e-3b19-e053-2995a90a3e8d.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 97 of 178 · 3,551 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71679-119-02 71679011902 200 TABLET in 1 BOTTLE (71679-119-02) 200 tablet 2025-06-18 0000-00-00 No No Current 71679-119-60 71679011960 60 TABLET in 1 BOTTLE (71679-119-60) 60 tablet 2025-06-18 No No Current