TIESO RAPIDO PLUS

Product NDC
73184-0083
Requested package NDC
73184-0083-1
11-digit product format
731840083
Labeler code
73184
Product ID
73184-0083_b927e5bd-3c87-444e-e053-2a95a90a34a1
Type
HUMAN OTC DRUG
Nonproprietary name
Homosalate, Ethylhexyl Salicylate, Titanium Dioxide, Benzalkonium Chloride
Dosage form
SPRAY
Route
TOPICAL
Labeler
ANDIVA Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-12-01
Marketing end
0000-00-00
Substance
HOMOSALATE; BENZALKONIUM CHLORIDE; TITANIUM DIOXIDE; OCTISALATE
Active strength
4 g/80mL; g/80mL; g/80mL; g/80mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 packagepackage73184-008373184-0083-1DDiscontinued 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#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73184-0083-1731840083011 BOTTLE, SPRAY in 1 BOX (73184-0083-1) > 80 mL in 1 BOTTLE, SPRAY2020-12-010000-00-00NoNoCurrent