Exuviance Daily Acne Peel

Product NDC: 58414-0017
11-digit product format: 584140017
Labeler code: 58414
Product ID: 58414-0017_2b593fd9-8310-5dc4-e063-6394a90ad6f3
Type: HUMAN OTC DRUG
Nonproprietary name: SALICYLIC ACID
Dosage form: LIQUID
Route: TOPICAL
Labeler: NeoStrata Company Inc.
Application: M006
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-06-15
Substance: SALICYLIC ACID
Active strength: 20 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	58414-0017	58414-0017-1	D	Discontinued by firm		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 · 20 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 package	package	58414-0017-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	58414-0017-1	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	58414-0017-1	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	58414-0017-1	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	58414-0017-1	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	58414-0017-1	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	58414-0017-1	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	58414-0017-1	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	58414-0017-1	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	58414-0017-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	58414-0017-1	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	58414-0017-1	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	58414-0017-1	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
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	58414-0017-2	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	58414-0017-2	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	58414-0017-2	I	Inactivated by FDA	`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: Exuviance Daily Acne Peel
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SALICYLIC ACID	20 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
O414PZ4LPZ	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
251577	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
e9f7da8a-c595-4500-89f1-ec8a2a72ef59	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
58414-0017-1	2022-05-02	Exuviance ® Daily Acne Peel
58414-0017-2	2022-05-02	Exuviance ® Daily Acne Peel
58414-0017-1	2021-01-29	Exuviance ® Daily Acne Peel
58414-0017-2	2021-01-29	Exuviance ® Daily Acne Peel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
58414-0017-1	Exuviance Daily Acne Peel	1 in 1 CARTON	LIQUID	1	6
58414-0017-1	Exuviance Daily Acne Peel	50 mL in 1 BOTTLE, PLASTIC	LIQUID	50	6
58414-0017-2	Exuviance Daily Acne Peel	100 mL in 1 BOTTLE, PLASTIC	LIQUID	100	6
58414-0017-2	Exuviance Daily Acne Peel	1 in 1 CARTON	LIQUID	1	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58414-0017	EXUVIANCE DAILY ACNE PEEL (SALICYLIC ACID) LIQUID [NEOSTRATA COMPANY INC.]	6	Current NDC, Legacy NDC, 4 package rows	20250112_e9f7da8a-c595-4500-89f1-ec8a2a72ef59.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 1 of 56 · 1,101 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Defense Acne Care 2% Salicylic Acid	SALICYLIC ACID 2%	Defense Soap LLC	98fcc243-d789-181d-e053-2995a90a9b5d	2026-09-09	Warnings	Exact identifier application number: M006
Jack Black Bump Fix	SALICYLIC ACID	Jack Black, L.L.C.	e8f51678-2675-405c-8462-351ec260051a	2026-09-08	Warnings	Exact identifier application number: M006
Abib Acne foam cleanser Heartleaf foam	SALICYLIC ACID	Fourcompany Co., Ltd.	5aa353ad-0ca5-77c1-e063-6394a90a6254	2026-09-04	Warnings	Exact identifier application number: M006
Dr.Leo Acne Buster Salicylic Acid Drying	SALICYLIC ACID	Doctor Leo USA Inc	5792fa71-eb6b-3c70-e063-6394a90abde8	2026-09-03	Warnings	Exact identifier application number: M006
Blackhead Clearing Scrug	SALICYLIC ACID	Walmart Inc.	6989591a-a78b-4971-baf2-51ebfaf9c7e7	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M006
Beisitian FACIAL BUMP REFINING ESSENCE	SALICYLIC ACID 2% FACIAL BUMP REFINING ESSENCE	Wenzhou Yuyuan Pharmaceutical Co., Ltd.	5a6784cd-93d3-aecc-e063-6294a90af021	2026-09-01	Warnings	Exact identifier application number: M006
Folliculitis Treatment Cream	BENZOYL PEROXIDE	Guangzhou Hechuang Commercial Service Co.,Ltd.	5a93f753-eb7d-ad11-e063-6294a90a6778	2026-09-01	Warnings	Exact identifier application number: M006
INVISIBLE ACNE PATCHES	SALICYLIC ACID 0.5%	Global America Group LLC	1527e15f-472f-4e05-adb6-c2e561f503cf	2026-08-31	Warnings	Exact identifier application number: M006
The Acne Spot Treatment	SALICYLIC ACID SPOT	Spotless, Inc.	4a1a3716-9eaf-6be4-e063-6294a90a31c3	2026-08-30	Warnings	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	Your Military Exchanges	57f06989-3ffa-4cd3-bde5-9d3cc639ac4d	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M006
Proactivplus Pore Clearing Treatment	SALICYLIC ACID	Alchemee, LLC	334efe89-3775-5ddb-e063-6294a90ae3a8	2026-08-27	Warnings	Exact identifier application number: M006
GENTLE ACNE CLEANSER	SALICYLIC ACID	Drmtlgy, LLC	2abed972-3fae-4ef0-abb6-1883457e98be	2026-08-26	Warnings	Exact identifier application number: M006
RAVN Mens Back Acne	SALICYLIC ACID	North Forge Brands LLC	4a512df2-4ad7-495c-868a-1f4d0a886391	2026-08-26	Warnings	Exact identifier application number: M006
Salicylic Acid Body Wash	SALICYLIC ACID	Guangdong Danlan International Biotechnology Co., Ltd	59d671e7-7bbc-a963-e063-6394a90a776f	2026-08-24	Warnings	Exact identifier application number: M006
Acne Scrub	SALICYLIC ACID	Walmart Inc.	5a76498e-a6f6-4e04-a2c7-245be947b006	2026-08-21	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Treatment Cream	BENZOYL PEROXIDE	CVS Health	aef82711-e3c3-439d-adda-542933ff4420	2026-08-19	Warnings	Exact identifier application number: M006
Tula Skincare Acne Heroes Acne Clearing Kit	SALICYLIC ACID	The Procter & Gamble Manufacturing Company	5967255f-b511-9c7f-e063-6294a90a3e63	2026-08-19	Warnings	Exact identifier application number: M006
BYT BANGYTONG MILIA REMOVER	SALICYLIC ACID 2% MILIA REMOVER	Shenzhen Jindali Technology Co., Ltd	596a2471-d07c-14a5-e063-6394a90a4fcc	2026-08-19	Warnings	Exact identifier application number: M006
RFA Clear and Calm Balancing Serum	SALICYLIC ACID	Topiderm, Inc.	f63f2c89-3567-4b08-be51-3fdfc5e0b1ba	2026-08-14	Warnings	Exact identifier application number: M006
WART REMOVER	SALICYLIC ACID	Shengnan (Guangzhou) Cosmetics Co., LTD	58e901b8-66e0-d2d6-e063-6394a90ae601	2026-08-13	Warnings	Exact identifier application number: M006

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O414PZ4LPZ	SALICYLIC ACID	69-72-7	SALICYLIC ACID

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
251577	salicylic acid 2 % Topical Solution	PSN	e9f7da8a-c595-4500-89f1-ec8a2a72ef59	6
251577	salicylic acid 20 MG/ML Topical Solution	SCD	e9f7da8a-c595-4500-89f1-ec8a2a72ef59	6
251577	salicylic acid 2 % Topical Solution	SY	e9f7da8a-c595-4500-89f1-ec8a2a72ef59	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
58414-0017-1	58414001701	1 in 1 CARTON					Historical
58414-0017-2	58414001702	1 BOTTLE, PLASTIC in 1 CARTON (58414-0017-2) / 100 mL in 1 BOTTLE, PLASTIC	2019-12-01	0000-00-00	No	No	Current