Home NDC 0363-0532 Mucus Relief
Product NDC 0363-0532
11-digit product format 003630532
Labeler code 0363
Product ID 0363-0532_830607df-ee15-46c4-9e1d-c7ac203029d4
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Walgreen Company
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-12-22
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 0363-0532-01 Mucus Relief 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 19 0363-0532-01 Mucus Relief 1 in 1 CARTON TABLET, FILM COATED 1 19 0363-0532-11 Mucus Relief 1 in 1 CARTON TABLET, FILM COATED 1 19 0363-0532-11 Mucus Relief 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 19 0363-0532-25 Mucus Relief 45 in 1 BOTTLE TABLET, FILM COATED 45 19 0363-0532-25 Mucus Relief 1 in 1 CARTON TABLET, FILM COATED 1 19 0363-0532-32 Mucus Relief 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 19 0363-0532-32 Mucus Relief 2 in 1 CARTON TABLET, FILM COATED 2 19
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0532 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [WALGREEN COMPANY] 18 Current NDC, Legacy NDC, 8 package rows 20250418_1cd69ede-29c6-4216-95b7-b58fc96c084b.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 · 3,550 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 0363-0532-01 00363053201 1 BOTTLE, PLASTIC in 1 CARTON (0363-0532-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-22 0000-00-00 No No Current 0363-0532-11 00363053211 1 BOTTLE, PLASTIC in 1 CARTON (0363-0532-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-22 0000-00-00 No No Current 0363-0532-25 00363053225 1 BOTTLE in 1 CARTON (0363-0532-25) > 45 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2005-12-22 0000-00-00 No No Current 0363-0532-32 00363053232 2 BOTTLE, PLASTIC in 1 CARTON (0363-0532-32) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-22 2028-08-31 No No Current