DermaFoam Premium Antibacterial

Product NDC
53125-709
11-digit product format
531250709
Labeler code
53125
Product ID
53125-709_ab987adb-b4df-8798-e053-2995a90a3de2
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOAP
Route
TOPICAL
Labeler
Superior Chemical
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-07-19
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 mg/mL
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct53125-709IInactivated by FDA2026-10-05
excluded productproduct53125-709DDiscontinued by firm2026-10-05
excluded packagepackage53125-70953125-709-39IInactivated by FDA2026-10-05
excluded packagepackage53125-70953125-709-29DDiscontinued by firm2026-10-05

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductDDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage53125-709-29DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductIInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage53125-709-29IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproductIInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage53125-709-29IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproductIInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage53125-709-29IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductIInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage53125-709-29IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductIInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage53125-709-29IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproductUExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage53125-709-29UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproductUExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage53125-709-29UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproductUExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage53125-709-29UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2025-01-30DermaFoam Premium Antibacterial
2024-10-01DermaFoam Premium Antibacterial
2024-07-30DermaFoam Premium Antibacterial
2024-01-30DermaFoam Premium Antibacterial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53125-709-39DermaFoam Premium Antibacterial1000 mL in 1 BAGSOAP10007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53125-709DERMAFOAM PREMIUM ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]7Legacy NDC, 1 package rows20241225_9a2fc005-5881-48c7-b2a3-3881ec88c2d1.zip
53125-709DERMAFOAM PREMIUM ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL]3Legacy NDC20200730_861a0cc3-90b6-0ffc-e053-2991aa0a7501.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN9a2fc005-5881-48c7-b2a3-3881ec88c2d17
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD9a2fc005-5881-48c7-b2a3-3881ec88c2d17
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY9a2fc005-5881-48c7-b2a3-3881ec88c2d17
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY9a2fc005-5881-48c7-b2a3-3881ec88c2d17

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53125-709-29531250709291000 mL in 1 BAG (53125-709-29) 1000 ml2017-07-190000-00-00NoNoCurrent
53125-709-39531250709391000 mL in 1 BAG1000 mlHistorical