FDA.reportPublic FDA data

BAC-D

Product NDC
86089-500
Requested package NDC
86089-500-17
11-digit product format
860890500
Labeler code
86089
Product ID
86089-500_9f3122d5-9c8f-4780-b74f-76f7e8324611
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
AEC Consumer Products, LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-01-01
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100mL
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 packagepackage86089-50086089-500-17IInactivated by FDA2026-08-03

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 · 11 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…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
86089-500-172024-07-30BAC-D Foaming Hand and Wound Sanitizer
86089-500-712024-07-30BAC-D Foaming Hand and Wound Sanitizer
86089-500-172024-01-30BAC-D Foaming Hand and Wound Sanitizer
86089-500-712024-01-30BAC-D Foaming Hand and Wound Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86089-500-17BAC-DFoaming Hand and Wound Sanitizer50 mL in 1 BOTTLE, PUMPLIQUID506
86089-500-71BAC-DFoaming Hand and Wound Sanitizer210 mL in 1 BOTTLE, PUMPLIQUID2106

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86089-500BAC-D FOAMING HAND AND WOUND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [AEC CONSUMER PRODUCTS, LLC]6Legacy NDC, 2 package rows20220104_1647db6d-a956-4123-b861-7a8b868629b7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1647db6d-a956-4123-b861-7a8b868629b76
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1647db6d-a956-4123-b861-7a8b868629b76
1020365benzalkonium chloride 0.13 % Topical FoamSY1647db6d-a956-4123-b861-7a8b868629b76

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
86089-500-178608905001750 mL in 1 BOTTLE, PUMP (86089-500-17) 50 ml2014-01-010000-00-00NoNoCurrent