Home NDC 72094-001-02 HylaTears
Product NDC 72094-001
Requested package NDC 72094-001-02
11-digit product format 720940001
Labeler code 72094
Product ID 72094-001_2b5fc4c4-843d-8d3d-e063-6394a90a5a1b
Type HUMAN OTC DRUG
Nonproprietary name Eye Drops
Dosage form LIQUID
Route OPHTHALMIC
Labeler Hyalogic LLC
Application M014
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-02-12
Substance HYPROMELLOSE 2910 (4000 MPA.S)
Active strength 3 mg/10mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base HylaTears
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYPROMELLOSE 2910 (4000 MPA.S) 3 mg/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RN3152OP35 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72094-001-01 HylaTears 20 mL in 1 BOTTLE, DROPPER LIQUID 20 5 72094-001-02 HylaTears 1 in 1 BOX LIQUID 1 5 72094-001-03 HylaTears 20 mL in 1 BOTTLE, DROPPER LIQUID 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72094-001 HYLATEARS (EYE DROPS) LIQUID [HYALOGIC LLC] 5 Current NDC, Legacy NDC, 2 package rows 20220211_64a30066-79a2-451d-e053-2991aa0ac68c.zip 72094-001 HYLATEARS (EYE DROPS) LIQUID [HYALOGIC LLC] 2 Current NDC, Legacy NDC, 1 package rows 20250123_2b5fc4c4-843c-8d3d-e063-6394a90a5a1b.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 1 of 7 · 136 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72094-001-02 72094000102 1 BOTTLE, DROPPER in 1 BOX (72094-001-02) > 20 mL in 1 BOTTLE, DROPPER (72094-001-01) 2018-02-12 0000-00-00 No No Current