Home NDC 73117-520 NebuClear MD
Product NDC 73117-520
11-digit product format 731170520
Labeler code 73117
Product ID 73117-520_518c7598-f182-9c72-e063-6394a90adc77
Type HUMAN OTC DRUG
Nonproprietary name Saline
Dosage form LIQUID
Route RESPIRATORY (INHALATION)
Labeler Blue Echo Care LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-01
Substance SODIUM CHLORIDE
Active strength 9 mg/9mg
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 NebuClear MD
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 9 mg/9mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII 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 73117-520-19 NebuClear MD 20 mg in 1 BOX LIQUID 20 2
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 74 of 180 · 3,583 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73117-520-19 73117052019 20 mg in 1 BOX (73117-520-19) 20 mg 2025-09-01 No No Current