FDA.reportPublic FDA data

North Woods Derma Foam E-2

Manufacturer
Superior Chemical Corporation | Betco corporation, Ltd.
Effective date
2019-04-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:59:04

Label at a glance#

ProductNorth Woods Derma Foam E-2
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredient

Benzalkonium Chloride 0.13%

INDICATIONS & USAGE SECTION

Uses

  • For handwashing to decrease the bacteria on the skin.
  • Recommended for repeated use.

WARNINGS SECTION

Warnings

  • For external use only.
  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
  • Stop use and ask a doctor If irritation persists or redness deelops, or if condition persists for more than 72 hours.
  • Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • ​Read the entire label before using this product.
  • ​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands for 15 seconds. Rinse with clean water.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

​Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

Superior Derma Foam E2

OTC - PURPOSE SECTION

Purpose

Antimicrobial

Superior Derma Foam E2

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Superior Derma Foam E2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71729-00 Superior Derma Foam71729-00 Superior Derma Foam

71729-00 Superior Derma Foam E2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53125-717-292024-10-01C16284748780-11030e365-1bb1-111a-e063-dadaa90a10e2North Woods Derma Foam E-2
53125-717-292024-07-30C16284748780-11030e365-1bb1-111a-e063-dadaa90a10e2North Woods Derma Foam E-2
53125-717-292024-01-30C16284748780-11030e365-1bb1-111a-e063-dadaa90a10e2North Woods Derma Foam E-2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53125-717NORTH WOODS DERMA FOAM E-2 (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]2Legacy NDC20190403_a91387c8-981e-43c7-a86e-26d02ba90aad.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53125-71753125-717-29

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO GLUCOSIDEICS790225BIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

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
4198c91f-342f-c5e5-e063-6294a90a2e76a91387c8-981e-43c7-a86e-26d02ba90aad2025-10-20WarningsExact identifier
spl set id: a91387c8-981e-43c7-a86e-26d02ba90aad

Reported adverse events (FAERS/openFDA)#

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