North Woods Derma Foam Hand Sanitizer

Product NDC: 53125-700
Requested package NDC: 53125-700-57
11-digit product format: 531250700
Labeler code: 53125
Product ID: 53125-700_408253ef-89cc-121e-e063-6294a90a24d4
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: 2015-10-01
Substance: BENZALKONIUM CHLORIDE
Active strength: 1.3 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	53125-700	53125-700-57	I	Inactivated by FDA		2026-08-10

Additional Listing Data#

Finished product: Yes
Brand name base: North Woods Derma Foam Hand Sanitizer
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	1.3 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F5UM2KM3W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1020365	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
ad51a175-2b91-fd14-e053-2995a90ad54d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
53125-700-54	2024-10-01	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-10-01	North Woods Derma Foam Hand Sanitizer
53125-700-54	2024-07-30	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-07-30	North Woods Derma Foam Hand Sanitizer
53125-700-54	2024-01-30	North Woods Derma Foam Hand Sanitizer
53125-700-57	2024-01-30	North Woods Derma Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
53125-700-29	North Woods Derma Foam Hand Sanitizer	1000 mL in 1 BAG	SOAP	1000	3
53125-700-88	North Woods Derma Foam Hand Sanitizer	500 mL in 1 BOTTLE, PUMP	SOAP	500	3
53125-700-54	North Woods Derma Foam Hand Sanitizer	1000 mL in 1 BAG	SOAP	1000	2
53125-700-57	North Woods Derma Foam Hand Sanitizer	550 mL in 1 BOTTLE, PUMP	SOAP	550	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53125-700	NORTH WOODS DERMA FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]	2	Current NDC, Legacy NDC, 2 package rows	20190410_861e2386-96cf-8b8e-e053-2991aa0ac57a.zip
53125-700	NORTH WOODS DERMA FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOAP [SUPERIOR CHEMICAL CORPORATION]	2	Current NDC, Legacy NDC, 2 package rows	20241228_ad51a175-2b91-fd14-e053-2995a90ad54d.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
North Woods Derma Foam Hand Sanitizer	BENZALKONIUM CHLORIDE	Superior Chemical Corporation	ad51a175-2b91-fd14-e053-2995a90ad54d	2025-10-06	Warnings	Exact identifier ndc (product): 53125-700

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	ad51a175-2b91-fd14-e053-2995a90ad54d	3
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	ad51a175-2b91-fd14-e053-2995a90ad54d	3
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	ad51a175-2b91-fd14-e053-2995a90ad54d	3
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	861e2386-96cf-8b8e-e053-2991aa0ac57a	2
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	861e2386-96cf-8b8e-e053-2991aa0ac57a	2
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	861e2386-96cf-8b8e-e053-2991aa0ac57a	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53125-700-57	53125070057	550 mL in 1 BOTTLE, PUMP (53125-700-57)	550 ml	2015-10-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
North Woods Derma Foam Hand Sanitizer	Superior Chemical Corporation \| Betco corporation, Ltd.	2025-10-06	HUMAN OTC DRUG LABEL	3
North Woods Derma Foam Hand Sanitizer	Superior Chemical Corporation \| Betco corporation, Ltd.	2019-04-09	HUMAN OTC DRUG LABEL	2