Home NDC 69790-010-32 ULINE Eyewash
Product NDC 69790-010
Requested package NDC 69790-010-32
11-digit product format 697900010
Labeler code 69790
Product ID 69790-010_14545fec-97fe-aed7-e063-6394a90a016d
Type HUMAN OTC DRUG
Nonproprietary name Eyewash
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Uline.
Application NDA022305
Marketing category NDA
Marketing start 2024-04-01
Substance WATER
Active strength 465 mL/473mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N022305-001 PUR-WASH PURIFIED WATER 98.3% SOLUTION / OPHTHALMIC RLD, RS 2011-09-01
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 N022305-001 PUR-WASH 98.3% SOLUTION / OPHTHALMIC RLD, RS 2011-09-01 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 2 · 22 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base ULINE Eyewash
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 465 mL/473mL
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 1151101 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 69790-010-16 ULINE Eyewash 473 mL in 1 BOTTLE, UNIT-DOSE SOLUTION 473 1 69790-010-32 ULINE Eyewash 946 mL in 1 BOTTLE, UNIT-DOSE SOLUTION 946 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69790-010 ULINE EYEWASH (EYEWASH) SOLUTION [ULINE.] 1 Current NDC, 2 package rows 20240402_14545fc9-1fb4-befa-e063-6294a90a0474.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69790-010-32 69790001032 946 mL in 1 BOTTLE, UNIT-DOSE (69790-010-32) 946 ml 2024-04-01 No No Current