ARTIFICIAL TEARS

Product NDC
70403-920
11-digit product format
704030920
Labeler code
70403
Product ID
70403-920_a8638cfd-ddd3-46c6-afcd-82a7f4119c5b
Type
HUMAN OTC DRUG
Nonproprietary name
Polyvinyl Alcohol
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Aru Pharma Inc.
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-03-31
Marketing end
0000-00-00
Substance
POLYVINYL ALCOHOL, UNSPECIFIED
Active strength
14 mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct70403-920DDiscontinued by firm2026-08-17
excluded packagepackage70403-92070403-920-15DDiscontinued by firm2026-08-17

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 · 10 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductDDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage70403-920-15DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductDDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage70403-920-15DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductIInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage70403-920-15IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproductIInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage70403-920-15IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductIInactivated by FDAbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage70403-920-15IInactivated by FDAbd6a592717d7…303034d00443…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70403-920-152023-05-15C16284748780-1d6a99b39-8870-a426-e053-dadaa90af4c2QPACK ARTIFICIAL TEARS
70403-920-152022-01-28C16284748780-1d6a99b39-8870-a426-e053-dadaa90af4c2QPACK ARTIFICIAL TEARS

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70403-920-15704030920151 BOTTLE, DROPPER in 1 CARTON (70403-920-15) > 15 mL in 1 BOTTLE, DROPPER2020-03-310000-00-00NoNoCurrent