FDA.reportPublic FDA data

Eye Wash

Product NDC
24208-070
Requested package NDC
24208-070-04
11-digit product format
242080070
Labeler code
24208
Product ID
24208-070_fb2fec84-9ad6-48aa-930f-8bd5078bb2d9
Type
HUMAN OTC DRUG
Nonproprietary name
water
Dosage form
SOLUTION
Route
OPHTHALMIC
Labeler
Bausch & Lomb Incorporated
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-08-31
Marketing end
0000-00-00
Substance
WATER
Active strength
99 mL/100mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage24208-07024208-070-04DDiscontinued by firm2026-10-05

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 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
WATERACTIVE INGREDIENT059QF0KO0REYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
WATERACTIVE MOIETY059QF0KO0REYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
BORIC ACIDINACTIVE INGREDIENTR57ZHV85D4EYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CBEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
SODIUM BORATEINACTIVE INGREDIENT91MBZ8H3QOEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2
SORBIC ACIDINACTIVE INGREDIENTX045WJ989BEYE WASH (WATER) SOLUTION [BAUSCH & LOMB INCORPORATED]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
24208-070-04242080070041 BOTTLE, PLASTIC in 1 CARTON (24208-070-04) > 118 mL in 1 BOTTLE, PLASTIC2010-08-310000-00-00NoNoCurrent