Antibacterial Wipes

Product NDC
70031-001
11-digit product format
700310001
Labeler code
70031
Product ID
70031-001_da8e3936-9206-730c-e053-2995a90a5a73
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
2015-08-05
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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2021-12-27 23:28 UTC · source 2021-12-27excluded productproduct8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-001-068dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-001-028dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-001-018dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-001-048dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage70031-001-038dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17excluded productproducte2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-001-06e2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-001-02e2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-001-01e2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-001-04e2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage70031-001-03e2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-001-069bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-001-029bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-001-019bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-001-049bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage70031-001-039bebd1f3094a…5416666fcb17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70031-001-017003100010112 POUCH in 1 BAG (70031-001-01) > .0108 g in 1 POUCH12 pouch2018-01-080000-00-00NoNoCurrent
70031-001-02700310001021 POUCH in 1 BAG (70031-001-02) > .0108 g in 1 POUCH1 pouch2018-01-080000-00-00NoNoCurrent
70031-001-03700310001031 POUCH in 1 BOTTLE, PLASTIC (70031-001-03) > .0108 g in 1 POUCH1 pouch2018-01-080000-00-00NoNoCurrent
70031-001-04700310001045 POUCH in 1 BAG (70031-001-04) > .0108 g in 1 POUCH5 pouch2018-01-080000-00-00NoNoCurrent
70031-001-06700310001066 POUCH in 1 BAG (70031-001-06) > .0108 g in 1 POUCH6 pouch2018-01-080000-00-00NoNoCurrent