Home NDC 68788-9858 Artificial Tears
Product NDC 68788-9858
11-digit product format 687889858
Labeler code 68788
Product ID 68788-9858_d81c8aec-ab42-4aa9-969c-4e5f19484b4a
Type HUMAN OTC DRUG
Nonproprietary name Polyvinyl Alcohol
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Preferred Pharmaceuticals, Inc
Application part349
Marketing category OTC MONOGRAPH FINAL
Marketing start 2012-03-13
Marketing end 0000-00-00
Substance POLYVINYL ALCOHOL, UNSPECIFIED
Active strength 14 mg/mL
NDC exclude flag No
Listing certified through 2019-12-31
Current FDA listing Historical FDA.report record 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 · 26 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 68788-9858-1 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 68788-9858-1 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 68788-9858-1 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 68788-9858-1 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 68788-9858-1 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 68788-9858-1 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 68788-9858-1 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 68788-9858-1 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68788-9858-1 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 68788-9858-1 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 68788-9858-1 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 68788-9858-1 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 68788-9858-1 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POLYVINYL ALCOHOL ACTIVE INGREDIENT 532B59J990 ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 POLYVINYL ALCOHOL ACTIVE MOIETY 532B59J990 ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 SODIUM PHOSPHATE, DIBASIC INACTIVE INGREDIENT GR686LBA74 ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 SODIUM PHOSPHATE, MONOBASIC INACTIVE INGREDIENT 3980JIH2SW ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ARTIFICIAL TEARS (POLYVINYL ALCOHOL) SOLUTION/ DROPS [PREFERRED PHARMACEUTICALS, INC] 1