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 23 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Redicare Alcohol Prep Pads	MEDIUM ALCOHOL PREP PADS	Redicare LLC	3cb7fba1-1d2d-f4da-e063-6394a90a4b21	2026-05-01	Warnings	Exact identifier application number: M003
SCOTT Antiseptic Foam Skin Cleanser	CHLOROXYLENOL	Kimberly-Clark	ca761935-7dcc-4caf-b941-60693a97c8a6	2026-04-30	Warnings	Exact identifier application number: M003
SCOTT FOAM HAND SANITIZER	BENZALKONIUM CHLORIDE	Kimberly-Clark	11234f21-04e4-4b16-88c3-51968a1cedca	2026-04-30	Warnings	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Retail Business Services, LLC	ad4e49b6-5784-4880-950b-6e6175fc312b	2026-04-30	Warnings, Adverse reactions	Exact identifier application number: M003
70%	ISOPROPYL ALCOHOL	Your Military Exchanges	3dcb8422-827d-479b-ba18-eee8dbb762e1	2026-04-30	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Target Corporation	33591569-8c56-4721-9d14-d9696f93c793	2026-04-30	Warnings, Adverse reactions	Exact identifier application number: M003
Oopsie 3 Hydrogen Peroxide	HYDROGEN PEROXIDE	4 Visions LLC	50b0d82a-da2c-5fd0-e063-6294a90aa165	2026-04-30	Warnings	Exact identifier application number: M003
Vita Vie Antibacterial Wash	BENZALKONIUM CHLORIDE	Spa De Soleil	a83883b7-9b63-641b-e053-2995a90ab943	2026-04-30	Warnings	Exact identifier application number: M003
Dr Lift Advanced Antibacterial Wipes	BENZALKONIUM CHLORIDE	Spa de Soleil	af89bd25-784e-4828-e053-2995a90a8aaa	2026-04-30	Warnings	Exact identifier application number: M003
Dr Lift Antibacterial Hand Wash	BENZALKONIUM CHLORIDE	Spa de Soleil	ab9e2c3c-d422-255e-e053-2a95a90a7a22	2026-04-30	Warnings	Exact identifier application number: M003
Dr Lift Antibacterial Body Scrub	BENZALKONIUM CHLORIDE	Spa de Soleil	ab9d6c73-29c1-036a-e053-2995a90a449c	2026-04-30	Warnings	Exact identifier application number: M003
KLEENEX Foam Hand Sanitizer	BENZALKONIUM CHLORIDE	Kimberly-Clark	1fa77ae2-b652-463d-8943-d338c591226e	2026-04-29	Warnings	Exact identifier application number: M003
Ethyl Rubbing Alcohol	ETHYL ALCOHOL	Your Military Exchanges	3dce175c-f893-4cfc-b495-6c11f2b77b87	2026-04-29	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Retail Business Services, LLC	2cc09239-a1d4-4276-adc4-82fdc396e23a	2026-04-29	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Perrigo Direct, Inc	11d89d11-103e-4ef6-a996-65cff67f9b32	2026-04-29	Warnings, Adverse reactions	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Walmart Inc.	1fd3d29f-7da0-c5ba-e063-6294a90add16	2026-04-29	Warnings, Adverse reactions	Exact identifier application number: M003
Ethyl Alcohol	ETHYL ALCOHOL	Walmart Inc.	1fd3bed0-8fcc-2cee-e063-6294a90a34fb	2026-04-29	Warnings, Adverse reactions	Exact identifier application number: M003
1438 DynaSoap	ANTIBACTERIAL HAND SOAP	Dynarex Corporation	ab0d5f64-9168-2ea3-e053-2a95a90a321e	2026-04-29	Warnings	Exact identifier application number: M003
SCOTT Antimicrobial Foam Skin Cleanser	BENZALKONIUM CHLORIDE	Kimberly-Clark	210f7da3-63c5-4a4b-8db0-8d6d1663751d	2026-04-28	Warnings	Exact identifier application number: M003
anzoon ANTISEPTIC WIPES	BENZETHONIUM CHLORIDE/BENZALKONIUM CHLORIDE	Shandong ACZ Biotechnology Co., Ltd.	506cd089-f9a7-d9e5-e063-6394a90af696	2026-04-27	Warnings	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