Home NDC 73117-522 NebuClear MD Saline
Product NDC 73117-522
11-digit product format 731170522
Labeler code 73117
Product ID 73117-522_55820ff9-7b4c-2bce-e063-6394a90a8b43
Type HUMAN OTC DRUG
Nonproprietary name NebuClear MD Saline
Dosage form LIQUID
Route NASAL
Labeler Blue Echo Care LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-30
Substance SODIUM CHLORIDE
Active strength 9 mg/mL
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 Saline
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 9 mg/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313000 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 29 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73117-522-21 73117052221 20 mL in 1 CARTON (73117-522-21) 20 ml 2026-06-01 No No Current 73117-522-22 73117052222 40 mL in 1 CARTON (73117-522-22) 40 ml 2026-06-30 No No Current 73117-522-23 73117052223 100 mL in 1 CARTON (73117-522-23) 100 ml 2026-06-30 No No Current