Home NDC 10956-059-30 DG Health Immediate Release Mucus Relief
Product NDC 10956-059
Requested package NDC 10956-059-30
11-digit product format 109560059
Labeler code 10956
Product ID 10956-059_1938e502-ee72-400d-933c-271efa88dc69
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin
Dosage form TABLET
Route ORAL
Labeler Reese Pharmaceutical Co
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-08-01
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 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 DG Health Immediate Release Mucus Relief
Listing expiration 2026-12-31 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10956-059-30 DG Health Immediate Release Mucus Relief 1 in 1 CARTON TABLET 1 3 10956-059-30 DG Health Immediate Release Mucus Relief 30 in 1 BOTTLE, PLASTIC TABLET 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10956-059 DG HEALTH IMMEDIATE RELEASE MUCUS RELIEF (GUAIFENESIN) TABLET [REESE PHARMACEUTICAL CO] 3 Current NDC, Legacy NDC, 2 package rows 20241220_f60a9d1b-7a63-43d3-b843-e1f31cf78873.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 98 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 10956-059-30 10956005930 1 BOTTLE, PLASTIC in 1 CARTON (10956-059-30) / 30 TABLET in 1 BOTTLE, PLASTIC 2013-12-01 0000-00-00 No No Current