United States · FDA National Drug Code directory

ULINE Eyewash

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69790-010_14545fec-97fe-aed7-e063-6394a90a016d
Product NDC
69790-010
Form
SOLUTION
Composition / generic term
Eyewash
Labeler
Uline.
Marketing category
NDA
Marketing start / end (source format)
20240401
Source listing expiry
20261231

Source-listed ingredients

  • WATER — 465 mL/473mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE, UNIT-DOSE (69790-010-16) · 69790-010-16
  • 946 mL in 1 BOTTLE, UNIT-DOSE (69790-010-32) · 69790-010-32

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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