FDA.reportPublic FDA data

ANTIBACTERIAL WET WIPES

Product NDC
79805-002
Requested package NDC
79805-002-03
11-digit product format
798050002
Labeler code
79805
Product ID
79805-002_ab2a99d4-c712-e427-e053-2995a90a2038
Type
HUMAN OTC DRUG
Nonproprietary name
ANTIBACTERIAL WET WIPES
Dosage form
CLOTH
Route
TOPICAL
Labeler
JUXIN (Jiangsu) New Material Packaging Co., Ltd.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/1001
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 packagepackage79805-00279805-002-03IInactivated by FDA2026-10-05

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 · 5 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08DDiscontinued by firmad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03DDiscontinued by firm367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09DDiscontinued by firm557ba5c1ecfa…9c80585c8c6e…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

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
79805-002-012022-07-2679805-002 ANTIBACTERIAL WET WIPES
79805-002-022022-07-2679805-002 ANTIBACTERIAL WET WIPES
79805-002-032022-07-2679805-002 ANTIBACTERIAL WET WIPES
79805-002-012022-01-2879805-002 ANTIBACTERIAL WET WIPES
79805-002-022022-01-2879805-002 ANTIBACTERIAL WET WIPES
79805-002-032022-01-2879805-002 ANTIBACTERIAL WET WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79805-002-01ANTIBACTERIAL WET WIPES15 in 1 BAGCLOTH153
79805-002-02ANTIBACTERIAL WET WIPES50 in 1 BAGCLOTH503
79805-002-03ANTIBACTERIAL WET WIPES75 in 1 BOTTLECLOTH753

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79805-002ANTIBACTERIAL WET WIPES CLOTH [JUXIN (JIANGSU) NEW MATERIAL PACKAGING CO., LTD.]3Legacy NDC, 3 package rows20250105_ab2aa8ce-8cf1-b8dc-e053-2995a90a212c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1812737benzalkonium Cl 0.3 % Medicated PadPSNab2aa8ce-8cf1-b8dc-e053-2995a90a212c3
1812737benzalkonium chloride 3 MG/ML Medicated PadSCDab2aa8ce-8cf1-b8dc-e053-2995a90a212c3
1812737benzalkonium chloride 0.3 % Medicated WipeSYab2aa8ce-8cf1-b8dc-e053-2995a90a212c3
1812737benzalkonium chloride 0.3 % Topical ClothSYab2aa8ce-8cf1-b8dc-e053-2995a90a212c3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79805-002-037980500020375 CLOTH in 1 BOTTLE (79805-002-03) 75 cloth2020-03-300000-00-00NoNoCurrent