TIESO SOL UV PROTECTOR

Product NDC
73184-0050
Requested package NDC
73184-0050-1
11-digit product format
731840050
Labeler code
73184
Product ID
73184-0050_b4c2a81b-c0a5-50b6-e053-2a95a90a4d7a
Type
HUMAN OTC DRUG
Nonproprietary name
Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Titanium Dioxide
Dosage form
CREAM
Route
TOPICAL
Labeler
ANDIVA Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-21
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; OCTINOXATE; OCTISALATE
Active strength
1 g/50mL; g/50mL; g/50mL
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage73184-005073184-0050-1DDiscontinued by firm2026-08-03

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…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73184-0050-12021-10-22C16284748780-1c7ccaba7-11e8-fd44-e053-dadaa90aa01bTIESO SOL UV PROTECTOR
73184-0050-12021-07-23C16284748780-1c7ccaba7-11e8-fd44-e053-dadaa90aa01bTIESO SOL UV PROTECTOR

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73184-0050-1731840050011 CONTAINER in 1 BOX (73184-0050-1) > 50 mL in 1 CONTAINER1 container2020-07-210000-00-00NoNoCurrent