Home NDC 72598-022 Plus Rinse Emergency Eyewash
Product NDC 72598-022
11-digit product format 725980022
Labeler code 72598
Product ID 72598-022_47e7bafd-1b4e-c454-e063-6394a90a6868
Type HUMAN OTC DRUG
Nonproprietary name Purified Water
Dosage form LIQUID
Route OPHTHALMIC
Labeler INNOVATIVE SAFETY SUPPLY INC.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-06
Substance WATER
Active strength 99.1 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 72598-022 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 72598-022 72598-022-20 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Plus Rinse Emergency Eyewash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 99.1 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72598-022-01 Plus Rinse Emergency Eyewash 1000 mL in 1 BOTTLE LIQUID 1000 7 72598-022-02 Plus Rinse Emergency Eyewash 200 mL in 1 BOTTLE LIQUID 200 7 72598-022-20 Plus Rinse Emergency Eyewash 500 mL in 1 BOTTLE LIQUID 500 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72598-022 PLUS RINSE EMERGENCY EYEWASH (PURIFIED WATER) LIQUID [INNOVATIVE SAFETY SUPPLY INC.] 6 Current NDC, Legacy NDC, 3 package rows 20240427_b3f47d26-39e4-4aea-bb92-358def52b652.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 72598-022-01 72598002201 1000 mL in 1 BOTTLE (72598-022-01) 1000 ml 2019-05-06 No No Current 72598-022-02 72598002202 200 mL in 1 BOTTLE (72598-022-02) 200 ml 2019-05-06 No No Current 72598-022-20 72598002220 500 mL in 1 BOTTLE (72598-022-20) 500 ml 2019-05-06 0000-00-00 No No Current