ANTIBACTERIAL

Product NDC: 41520-281
11-digit product format: 415200281
Labeler code: 41520
Product ID: 41520-281_5bb51652-ea78-4727-91c3-2e94e7cc4abe
Type: HUMAN OTC DRUG
Nonproprietary name: TRICLOSAN
Dosage form: LIQUID
Route: TOPICAL
Labeler: AMERICAN SALES COMPANY
Application: part333E
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2011-06-22
Marketing end: 0000-00-00
Substance: TRICLOSAN
Active strength: 0 mL/100mL
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	41520-281		I	Inactivated by FDA		2026-10-05
excluded package	package	41520-281	41520-281-08	I	Inactivated by FDA		2026-10-05

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 · 44 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	41520-281-08	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	41520-281-08	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	41520-281-08	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	41520-281-08	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	41520-281-08	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	41520-281-08	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	41520-281-08	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	41520-281-08	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	41520-281-08	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	41520-281-08	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	41520-281-08	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	41520-281-08	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	41520-281-08	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	41520-281-08	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	41520-281-08	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41520-281-08	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41520-281-08	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41520-281-08	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41520-281-08	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	41520-281-08	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	41520-281-08	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	41520-281-08	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
1681bc73-b05f-12c3-1075-382ae39f449c	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
41520-281-08	2020-01-31	C162847	48780-1	9d75b9d0-8977-f424-e053-dadaa90a57ce	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41520-281-08	ANTIBACTERIAL	236 mL in 1 BOTTLE, PUMP	LIQUID	236		1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
TRICLOSAN	ACTIVE MOIETY	4NM5039Y5X	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
ALANINE	INACTIVE INGREDIENT	OF5P57N2ZX	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
ARGININE	INACTIVE INGREDIENT	94ZLA3W45F	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
BETAINE	INACTIVE INGREDIENT	3SCV180C9W	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
COCAMIDOPROPYL BETAINE	INACTIVE INGREDIENT	5OCF3O11KX	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
CRANBERRY	INACTIVE INGREDIENT	0MVO31Q3QS	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
EDETATE SODIUM	INACTIVE INGREDIENT	MP1J8420LU	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
GLUTAMIC ACID	INACTIVE INGREDIENT	3KX376GY7L	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
GLYCINE	INACTIVE INGREDIENT	TE7660XO1C	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
LYSINE	INACTIVE INGREDIENT	K3Z4F929H6	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
METHYLCHLOROISOTHIAZOLINONE	INACTIVE INGREDIENT	DEL7T5QRPN	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
METHYLISOTHIAZOLINONE	INACTIVE INGREDIENT	229D0E1QFA	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
PEG-120 METHYL GLUCOSE DIOLEATE	INACTIVE INGREDIENT	YM0K64F20V	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
PEG-7 GLYCERYL COCOATE	INACTIVE INGREDIENT	VNX7251543	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
POMEGRANATE	INACTIVE INGREDIENT	56687D1Z4D	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
PROLINE	INACTIVE INGREDIENT	9DLQ4CIU6V	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
SERINE	INACTIVE INGREDIENT	452VLY9402	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
SODIUM LAURETH SULFATE	INACTIVE INGREDIENT	BPV390UAP0	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
SODIUM PYRROLIDONE CARBOXYLATE	INACTIVE INGREDIENT	469OTG57A2	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
THREONINE	INACTIVE INGREDIENT	2ZD004190S	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41520-281	ANTIBACTERIAL (TRICLOSAN) LIQUID [AMERICAN SALES COMPANY]	1	Legacy NDC, 1 package rows	20110624_73f727ce-2fcc-4de5-b753-8f675d4aef7e.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4NM5039Y5X	TRICLOSAN	3380-34-5	TRICLOSAN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1020118	triclosan 0.15 % Medicated Liquid Soap	PSN	73f727ce-2fcc-4de5-b753-8f675d4aef7e	1
1020118	triclosan 1.5 MG/ML Medicated Liquid Soap	SCD	73f727ce-2fcc-4de5-b753-8f675d4aef7e	1
1020118	triclosan 0.15 % Medicated Liquid Soap	SY	73f727ce-2fcc-4de5-b753-8f675d4aef7e	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
41520-281-08	41520028108	236 mL in 1 BOTTLE, PUMP	236 ml	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DRUG FACTS	AMERICAN SALES COMPANY \| APOLLO HEALTH AND BEAUTY CARE	2011-06-22	HUMAN OTC DRUG LABEL	1