Dermal Wound Cleanser

Product NDC: 69740-490
11-digit product format: 697400490
Labeler code: 69740
Product ID: 69740-490_1d4e61fc-0bf2-fb51-e063-6294a90a21fe
Type: HUMAN OTC DRUG
Nonproprietary name: BENZETHONIUM CHLORIDE
Dosage form: SPRAY
Route: TOPICAL
Labeler: Smith & Nephew Medical Ltd.
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1994-04-01
Substance: BENZETHONIUM CHLORIDE
Active strength: 1.3 g/981mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 8 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69740-490-00	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69740-490-00	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69740-490-00	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69740-490-00	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Dermal Wound Cleanser
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZETHONIUM CHLORIDE	1.3 g/981mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
PH41D05744	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
582205	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
18704cd5-1ecf-4e8c-9897-7e45394e68c8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906	Product name	7	20210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69740-490-00	2024-07-15	C162847	48780-1	f386c64a-2b85-0266-e053-dadaa90a7c1a	Dermal Wound Cleanser
69740-490-00	2023-01-30	C162847	48780-1	f386c64a-2b85-0266-e053-dadaa90a7c1a	Dermal Wound Cleanser

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69740-490-00	Dermal Wound Cleanser	473 mL in 1 BOTTLE, SPRAY	SPRAY	473		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZETHONIUM CHLORIDE	ACTIVE INGREDIENT	PH41D05744	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
BENZETHONIUM	ACTIVE MOIETY	1VU15B70BP	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
POLYSORBATE 20	INACTIVE INGREDIENT	7T1F30V5YH	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69740-490	DERMAL WOUND CLEANSER (BENZETHONIUM CHLORIDE) SPRAY [SMITH & NEPHEW MEDICAL LTD.]	5	Current NDC, Legacy NDC, 1 package rows	20240716_18704cd5-1ecf-4e8c-9897-7e45394e68c8.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 30 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand Sanitizer	ALCOHOL	Trifecta Pharmaceuticals USA	0ba469a8-53f3-eb8e-e063-6294a90a1efc	2026-03-04	Warnings	Exact identifier application number: M003
Isopropyl alcohol 91 percent ReadyInCase	ISOPROPYL ALCOHOL	P & L Development, LLC	a6d2068f-705d-4341-b1c8-81e1b563ab9a	2026-03-04	Warnings	Exact identifier application number: M003
50% Isopropyl Alcohol	ISOPROPYL ALCOHOL	Amazon.com Services LLC	95e31119-8487-4bc9-b1c2-c43d32fc80ce	2026-03-03	Warnings, Adverse reactions	Exact identifier application number: M003
FOOTSPA PEDI	ALCOHOL	CHEMCO CORPORATION	3886a958-d035-ed15-e063-6294a90af1b5	2026-03-03	Warnings	Exact identifier application number: M003
Medicated Apricot Scrub	SALICYLIC ACID	Old East Main Co.	7c9c430b-30d8-4642-85bd-d028a9aa748a	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Old East Main Co.	fb9bbb51-d131-42b4-94e6-b752595b1081	2026-03-02	Warnings	Exact identifier application number: M003
Isopropyl	ISOPROPYL ALCOHOL	Old East Main Co.	ea6f3065-780e-4afc-a361-a2cb296ae4d5	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Old East Main Co.	2a09f6c0-e9a6-4f48-bce1-6cf7345f2d87	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
70%	ISOPROPYL ALCOHOL	Old East Main Co.	3e7a7f3e-3e99-4999-95c2-1603aca08e89	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
50% Rubbing	ISOPROPYL ALCOHOL	Old East Main Co.	2b600254-2a70-4254-85fb-29b9adb56c9a	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Old East Main Co.	3c823b47-2ab7-4002-9b6f-abf0a3176b44	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M003
American Red Cross 6oz, 3% Hydrogen Peroxide	AMERICAN RED CROSS 6 OZ, 3% HYDROGEN PEROXIDE SPRAY	MY IMPORTS USA LLC	29299c46-a929-0d92-e063-6294a90a4218	2026-03-02	Warnings	Exact identifier application number: M003
Isopropyl alcohol 91 percent	ISOPROPYL ALCOHOL	TARGET Corporation	c49f46c5-f9b2-4045-a31d-63cb22210233	2026-03-02	Warnings	Exact identifier application number: M003
Isopropyl alcohol 91 percent	ISOPROPYL ALCOHOL	Sam's West, Inc	a9d6778a-e5ad-4e02-9142-4a932540eda7	2026-03-02	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Chain Drug Marketing Association	31e7063e-0ba1-434f-b404-0ec42df634a3	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M003
Iodine Tincture	IODINE TINCTURE	The Kroger Co.	c70a718f-d51a-455a-9785-ab41c1b1f8b0	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M003
MedPride Sterile	BENZALKONIUM CHLORIDE	Shield Line LLC	02f63d50-e4ff-49b6-9f8c-fddceefe65f3	2026-02-27	Warnings	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Walmart Inc.	c8fa5ed3-0497-4a23-934b-c72ff02c94ae	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M003
FIGS - evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented	ETHYL ALCOHOL	WE EVOLVETOGETHER INC.	4bd5a36d-06b4-ba41-e063-6294a90aa121	2026-02-27	Warnings	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	United Natural Foods, Inc. dba UNFI	4eee73dd-039e-44a5-b380-21ff32efee22	2026-02-26	Warnings, Adverse reactions	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
PH41D05744	BENZETHONIUM CHLORIDE	121-54-0	BENZETHONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
582205	benzethonium chloride 0.13 % Topical Spray	PSN	18704cd5-1ecf-4e8c-9897-7e45394e68c8	5
582205	benzethonium chloride 1.3 MG/ML Topical Spray	SCD	18704cd5-1ecf-4e8c-9897-7e45394e68c8	5
582205	benzethonium chloride 0.13 % Topical Spray	SY	18704cd5-1ecf-4e8c-9897-7e45394e68c8	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69740-490-00	69740049000	473 mL in 1 BOTTLE, SPRAY (69740-490-00)	473 ml	1994-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Dermal Wound Cleanser	Smith & Nephew Medical Ltd. \| Swiss-American CDMO, LLC	2024-07-15	HUMAN OTC DRUG LABEL	5