North Woods Derma Foam E-2

Product NDC: 53125-717
11-digit product format: 531250717
Labeler code: 53125
Product ID: 53125-717_85908601-0c5a-395f-e053-2a91aa0a8d0f
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: SOAP
Route: TOPICAL
Labeler: Superior Chemical Corporation
Application: part333A
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2016-09-15
Marketing end: 0000-00-00
Substance: BENZALKONIUM CHLORIDE
Active strength: 1 mg/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	53125-717		D	Discontinued by firm		2026-10-16
excluded package	package	53125-717	53125-717-29	D	Discontinued by firm		2026-10-16

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product	53125-717		D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	53125-717	53125-717-29	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53125-717-29	2024-10-01	C162847	48780-1	1030e365-1bb1-111a-e063-dadaa90a10e2	North Woods Derma Foam E-2
53125-717-29	2024-07-30	C162847	48780-1	1030e365-1bb1-111a-e063-dadaa90a10e2	North Woods Derma Foam E-2
53125-717-29	2024-01-30	C162847	48780-1	1030e365-1bb1-111a-e063-dadaa90a10e2	North Woods Derma Foam E-2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53125-717	NORTH WOODS DERMA FOAM E-2 (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]	2	Legacy NDC	20190403_a91387c8-981e-43c7-a86e-26d02ba90aad.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53125-717-29	53125071729	1000 mL in 1 BAG (53125-717-29)	1000 ml	2016-09-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
North Woods Derma Foam E-2	Superior Chemical Corporation \| Betco corporation, Ltd.	2019-04-02	HUMAN OTC DRUG LABEL	2