Benzethonium chloride Plus Dyclonine hydrochloride

Product NDC: 41520-089
11-digit product format: 415200089
Labeler code: 41520
Product ID: 41520-089_4093bca2-05f8-a063-e063-6394a90a8041
Type: HUMAN OTC DRUG
Nonproprietary name: Liquid Bandage
Dosage form: LIQUID
Route: TOPICAL
Labeler: Foodhold USA
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-12-19
Substance: BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength: .2; .75 mg/9mL; mg/9mL
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
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41520-089-03	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41520-089-03	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41520-089-03	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41520-089-03	`8dfbde2a14a4…`	`c9ff85d89658…`

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: Benzethonium chloride Plus Dyclonine hydrochloride
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZETHONIUM CHLORIDE	.2 mg/9mL
DYCLONINE HYDROCHLORIDE	.75 mg/9mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
PH41D05744	Internal UNII lookup
ZEC193879Q	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
1e897ee5-17e3-459e-88e3-d7436ee22f37	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
1da7d10e-498b-41dd-970f-0f5bd7432f39	Product name	1	20190228

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-01-12	CareOne Liquid Bandage
2023-01-12	CareOne Liquid Bandage
2021-07-23	CareOne Liquid Bandage
2021-07-23	CareOne Liquid Bandage

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41520-089-03	Benzethonium chloride Plus Dyclonine hydrochloride	9 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	9		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41520-089	BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [FOODHOLD USA]	6	Current NDC, Legacy NDC, 1 package rows	20241109_1e897ee5-17e3-459e-88e3-d7436ee22f37.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 115 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
ZEC193879Q	DYCLONINE HYDROCHLORIDE	536-43-6	DYCLONINE HYDROCHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41520-089-03	41520008903	9 mL in 1 BOTTLE, WITH APPLICATOR (41520-089-03)	9 ml	2017-12-19	0000-00-00	No	No	Current