Antibacterial Wet Wipes

Product NDC
70031-003
Requested package NDC
70031-003-02
11-digit product format
700310003
Labeler code
70031
Product ID
70031-003_da8daf04-fa21-2ea3-e053-2a95a90a2761
Type
HUMAN OTC DRUG
Nonproprietary name
benzethonium chloride
Dosage form
SWAB
Route
TOPICAL
Labeler
TIANJIN YANSHENG INDUSTRIAL TRADE COMPANY
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-03-10
Marketing end
0000-00-00
Substance
BENZETHONIUM CHLORIDE
Active strength
0 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
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 · 3 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-00370031-003-02IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-00370031-003-02IInactivated by FDAexcluded / ndc_excluded.zipe2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-00370031-003-02IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70031-003-027003100030210 POUCH in 1 PACKAGE (70031-003-02) > 3 g in 1 POUCH10 pouch2018-01-080000-00-00NoNoCurrent