FDA.reportPublic FDA data

MEDIF WHITE TOOTH

Product NDC
72346-120
Requested package NDC
72346-120-02
11-digit product format
723460120
Labeler code
72346
Product ID
72346-120_4b01d8d9-7429-4981-93d7-38ead4d82135
Type
HUMAN OTC DRUG
Nonproprietary name
Hydrated Silica, Aluminium Chlorohydrate, Allantoinate
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Labeler
MEDIF CO.,LTD
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-10-01
Marketing end
0000-00-00
Substance
HYDRATED SILICA; ALUMINUM CHLOROHYDRATE; ALLANTOIN
Active strength
17 g/130g; g/130g; g/130g
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 packagepackage72346-12072346-120-02DDiscontinued by firm2026-10-05

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 · 8 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31DDiscontinued by firm2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28DDiscontinued by firma1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21DDiscontinued by firmcfe11265f3b6…090c488252e2…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72346-120-022025-03-10C16284748780-12cef2736-7ef0-d83d-e063-dadaa90ab31ffe1237e5-57cb-43b6-a9c6-cea550f2c87b
72346-120-022025-01-30C16284748780-12cef2736-7ef0-d83d-e063-dadaa90ab31ffe1237e5-57cb-43b6-a9c6-cea550f2c87b

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72346-120-02723460120021 TUBE in 1 CARTON (72346-120-02) > 130 g in 1 TUBE (72346-120-01) 1 tube2020-10-010000-00-00NoNoCurrent