FDA.reportPublic FDA data

Antibacterial Wet Wipes

Product NDC
70888-001
Requested package NDC
70888-001-09
11-digit product format
708880001
Labeler code
70888
Product ID
70888-001_da8e3936-9205-730c-e053-2995a90a5a73
Type
HUMAN OTC DRUG
Nonproprietary name
benzalkonium chloride
Dosage form
SWAB
Route
TOPICAL
Labeler
SHAOXING BAIXUN HYGIENE PRODUCTS CO.,LTD
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-08-06
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage70888-00170888-001-09DDiscontinued by firm2026-10-15

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…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
70888-001-012022-03-19Antibacterial Wet Wipes
70888-001-022022-03-19Antibacterial Wet Wipes
70888-001-032022-03-19Antibacterial Wet Wipes
70888-001-042022-03-19Antibacterial Wet Wipes
70888-001-052022-03-19Antibacterial Wet Wipes
70888-001-062022-03-19Antibacterial Wet Wipes
70888-001-072022-03-19Antibacterial Wet Wipes
70888-001-082022-03-19Antibacterial Wet Wipes
70888-001-092022-03-19Antibacterial Wet Wipes
70888-001-102022-03-19Antibacterial Wet Wipes
70888-001-012022-01-28Antibacterial Wet Wipes
70888-001-022022-01-28Antibacterial Wet Wipes
70888-001-032022-01-28Antibacterial Wet Wipes
70888-001-042022-01-28Antibacterial Wet Wipes
70888-001-052022-01-28Antibacterial Wet Wipes
70888-001-062022-01-28Antibacterial Wet Wipes
70888-001-072022-01-28Antibacterial Wet Wipes
70888-001-082022-01-28Antibacterial Wet Wipes
70888-001-092022-01-28Antibacterial Wet Wipes
70888-001-102022-01-28Antibacterial Wet Wipes

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70888-001-097088800010980 POUCH in 1 BOTTLE (70888-001-09) > .336 g in 1 POUCH80 pouch2016-08-060000-00-00NoNoCurrent