Home NDC 51316-709-45 CVS ULTRA FINE MOISTURIZING SALINE MIST
Product NDC 51316-709
Requested package NDC 51316-709-45
11-digit product format 513160709
Labeler code 51316
Product ID 51316-709_498b51c1-993d-e4dd-e063-6294a90a82de
Type HUMAN OTC DRUG
Nonproprietary name NASAL MIST
Dosage form AEROSOL, SPRAY
Route NASAL
Labeler CVS
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-01-29
Substance SODIUM CHLORIDE
Active strength .9 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base CVS ULTRA FINE MOISTURIZING SALINE MIST
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE .9 g/100mL
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 351179 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 51316-709-45 CVS ULTRA FINE MOISTURIZING SALINE MIST 142 mL in 1 BOTTLE, SPRAY AEROSOL, SPRAY 142 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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51316-709-45 51316070945 142 mL in 1 BOTTLE, SPRAY (51316-709-45) 142 ml 2026-01-29 No No Current