Dermal Wound Cleanser

Product NDC: 69740-492
11-digit product format: 697400492
Labeler code: 69740
Product ID: 69740-492_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: 1991-04-01
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	69740-492-00	`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	69740-492-00	`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	69740-492-00	`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	69740-492-00	`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
69740-492-00	2024-07-15	C162847	48780-1	f386c64a-2b85-0266-e053-dadaa90a7c1a	Dermal Wound Cleanser
69740-492-00	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
69740-492-00	Dermal Wound Cleanser	236 mL in 1 BOTTLE, SPRAY	SPRAY	236		5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69740-492-00	ML - Milliliter	69740-492	b4861653-0c37-469c-a255-865ed7dc304d	1	2025-01-14

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
69740-492	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 114 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Henry Schein Povidone-Iodine Swabsticks	POVIDONE-IODINE	Henry Schein, Inc.	5854f241-6cfc-4e5a-ba72-92dd0703f728	2023-10-13	Warnings	Exact identifier application number: M003
DawnMist Alcohol Hand Sanitizer	ALCOHOL	Dukal LLC	a2df96a9-8514-6839-e053-2a95a90a9417	2023-10-13	Warnings	Exact identifier application number: M003
DUKAL STING RELIEF PAD	BENZOCAINE	Dukal LLC	67c1ddc7-8fde-4431-84cb-f757682d5f3e	2023-10-13	Warnings	Exact identifier application number: M003
First Aid Only First Aid/Burn	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	Acme United Corporation	07245b54-b193-178e-e063-6394a90a2581	2023-10-09	Warnings	Exact identifier application number: M003
Hand sanitizer 2oz 2pk original	ETHYL ALCOHOL	Rejoice International Corp.	06dc1730-216a-8b4d-e063-6294a90a4184	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 1.8oz with extra clip original	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	06dcf8dc-0831-475e-e063-6394a90a9fef	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 2oz 2pk original	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	06dd2427-097c-b0fa-e063-6294a90a4f82	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 1.8oz with extra clip original	ETHYL ALCOHOL	Rejoice International Corp.	06da0cc1-95f2-4f88-e063-6394a90a25ea	2023-10-03	Warnings	Exact identifier application number: M003
First Aid Antiseptic Alcohol Pads Isopropyl Alcohol 70 Rite Aid	ISOPROPYL ALCOHOL	Rite Aid Corporation	aa0df5fe-62d1-407d-b8f9-a7fd9473d569	2023-10-02	Warnings	Exact identifier application number: M003
Foaming Instant Hand Sanitizer with Aloe	ETHANOL	MCKESSON MEDICAL-SURGICAL INC.	5c1f69b7-c8d8-477c-b614-47a3287b0e4c	2023-06-05	Warnings	Exact identifier application number: M003
Bactine Max Dry	LIDOCAINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	466404cd-c46a-4944-b1ac-3b3b17f436a1	2022-12-27	Warnings	Exact identifier application number: M003
Povidone-Iodine Pad	POVIDONE-IODINE	Shandong Haiyan Medical Manufacture Co., Ltd.	c9187a07-92d5-15ac-e053-2995a90af4cb	2022-03-19	Warnings	Exact identifier application number: M003
Alcohol Prep Pad	ISOPROPYL ALCOHOL	Shandong Haiyan Medical Manufacture Co., Ltd.	1a117840-22d0-4a88-b1a6-e43162a444ab	2022-03-19	Warnings	Exact identifier application number: M003
FIRSTAR BZK Antiseptic Towelette	BENZALKONIUM CHLORIDE	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	28591a97-9291-48c8-a8e3-c419180331b3	2021-07-06	Warnings	Exact identifier application number: M003
Bactine Max	BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	28e8a311-20a4-45a1-8d5d-ca42b101c275	2021-02-24	Warnings	Exact identifier application number: M003
Hand Sanitizer Lemon 2oz	ALCOHOL	Ningbo Rejoice International	b0a4159a-cb07-4ce6-e053-2995a90a76e7	2020-10-02	Warnings	Exact identifier application number: M003
Sanix Alcohol Hand Rub	ALCOHOL	Topiderm, Inc	a4fbb714-4f20-400a-ab98-f1c8807ce6fc	2020-03-24	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
69740-492-00	69740049200	236 mL in 1 BOTTLE, SPRAY (69740-492-00)	236 ml	1991-04-01	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