Home NDC 24208-005 Advanced Eye Relief Eye Wash
Product NDC 24208-005
11-digit product format 242080005
Labeler code 24208
Product ID 24208-005_2e5ebd4d-dda3-1a52-e063-6394a90a7e29
Type HUMAN OTC DRUG
Nonproprietary name water solution
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Bausch & Lomb Incorporated
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-02-02
Substance WATER
Active strength 99.05 mL/100mL
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 Advanced Eye Relief Eye Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 99.05 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 059QF0KO0R Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053429 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 24208-005-04 Advanced Eye Relief Eye Wash 118 mL in 1 APPLICATOR SOLUTION/ DROPS 118 6 24208-005-04 Advanced Eye Relief Eye Wash 1 in 1 CARTON SOLUTION/ DROPS 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24208-005 ADVANCED EYE RELIEF EYE WASH (WATER SOLUTION) SOLUTION/ DROPS [BAUSCH & LOMB INCORPORATED] 6 Current NDC, Legacy NDC, 2 package rows 20250221_9caccce1-4530-441d-bf76-244edeb9dedc.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 6 of 25 · 494 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 24208-005-04 24208000504 1 APPLICATOR in 1 CARTON (24208-005-04) / 118 mL in 1 APPLICATOR 1 applicator 2017-02-02 0000-00-00 No No Current