North Woods Derma Foam E-2

Product NDC
53125-817
11-digit product format
531250817
Labeler code
53125
Product ID
53125-817_2736622c-4ecb-472d-e063-6394a90aa9db
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOAP
Route
TOPICAL
Labeler
Superior Chemical Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-09-15
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
North Woods Derma Foam E-2
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.3 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046593Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
ab982dec-639a-277a-e053-2a95a90ac8b4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53125-817-292024-10-01C16284748780-11030e365-22ee-111a-e063-dadaa90a10e2North Woods Derma Foam E-2
53125-817-292024-07-30C16284748780-11030e365-22ee-111a-e063-dadaa90a10e2North Woods Derma Foam E-2
53125-817-292024-01-30C16284748780-11030e365-22ee-111a-e063-dadaa90a10e2North Woods Derma Foam E-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53125-817-29North Woods Derma Foam E-21000 mL in 1 BAGSOAP10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53125-817NORTH WOODS DERMA FOAM E-2 (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]2Current NDC, Legacy NDC, 1 package rows20241120_ab982dec-639a-277a-e053-2a95a90ac8b4.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
North Woods Derma Foam E-2BENZALKONIUM CHLORIDESuperior Chemical Corporationab982dec-639a-277a-e053-2a95a90ac8b42024-11-18WarningsExact identifier
ndc (product): 53125-817

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSNab982dec-639a-277a-e053-2a95a90ac8b42
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCDab982dec-639a-277a-e053-2a95a90ac8b42
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSYab982dec-639a-277a-e053-2a95a90ac8b42
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSYab982dec-639a-277a-e053-2a95a90ac8b42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53125-817-29531250817291000 mL in 1 BAG (53125-817-29) 1000 ml2016-09-150000-00-00NoNoCurrent