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		2026-10-16

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 5 of 55 · 1,088 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
10% Azelaic Acid	AZELAIC ACID CREAM	Guangzhou Ariel Medical Technology Co., Ltd.	55b03daa-b6d4-9edf-e063-6394a90ac4d1	2026-07-03	Warnings	Exact identifier application number: M006
Hero Mighty Cleanser	SALICYLIC ACID	Church & Dwight Co., Inc.	5597df54-2e58-0d6a-e063-6394a90a1697	2026-07-01	Warnings	Exact identifier application number: M006
Hero Pore Cleanser	SALICYLIC ACID	Church & Dwight Co., Inc.	559987c0-7abe-13fc-e063-6294a90a9f27	2026-07-01	Warnings	Exact identifier application number: M006
Acne Treatment Cream	2% SALICYLIC ACID	Zytrell Skin Solutions Inc.	555be487-92d8-6220-e063-6394a90a0c0a	2026-06-28	Warnings	Exact identifier application number: M006
SKINTIFIC 3X ACID INTENSIVE ACNE TREATMENT	SALICYLIC ACID	Longway Technology(Guangzhou)Co., Ltd.	553957ef-cb8a-e75d-e063-6394a90a261b	2026-06-27	Warnings	Exact identifier application number: M006
ORLASKIN ACNE Treatment	SALICYLIC ACID	Guangzhou Yapheon Health Industry Co., Ltd.	552bf5df-0a3c-7c10-e063-6394a90a311f	2026-06-26	Warnings	Exact identifier application number: M006
ORLASKIN SALICYLIC ACID ACNE TREATMENT PADS	SALICYLIC ACID	Guangzhou Yapheon Health Industry Co., Ltd.	552c9e72-db4b-641a-e063-6294a90a2901	2026-06-26	Warnings	Exact identifier application number: M006
CosmoClear Cleanser	SALICYLIC ACID	Noon Aesthetics M.R. Ltd	dd738dfd-676b-40fe-8b0e-3d8305e0fdcb	2026-06-25	Warnings	Exact identifier application number: M006
Walgreens Acne Foaming Cleanser	BENZOYL PEROXIDE	WALGREEN COMPANY	549fddb8-9d42-16cb-e063-6294a90aa2a9	2026-06-19	Warnings	Exact identifier application number: M006
Walgreens Maximum Strength Acne Treatment	BENZOYL PEROXIDE	WALGREEN COMPANY	548e327b-1a4f-03df-e063-6294a90a3932	2026-06-18	Warnings	Exact identifier application number: M006
Epoch	SALICYLIC ACID	NSE Products, Inc.	3084ac37-de1f-4218-9471-6a5ebf720eb9	2026-06-17	Warnings	Exact identifier application number: M006
VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER	SALICYLIC ACID	LOreal USA Products Inc	17b7a58b-97f2-429f-83cb-db04631d307d	2026-06-16	Warnings	Exact identifier application number: M006
VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER	SALICYLIC ACID	Cosmetique Active Production	17b8a58b-97f2-429f-83cb-db04631d307d	2026-06-16	Warnings	Exact identifier application number: M006
Societe Clarity Bac	SALICYLIC ACID	Societe Clinical Skincare	545130ce-46f9-c231-e063-6394a90a1ea8	2026-06-16	Warnings	Exact identifier application number: M006
ES Salicylic Wash	SALICYLIC ACID	Elaine Sterling Enterprises	543ab052-5aa9-6585-e063-6394a90af88f	2026-06-16	Warnings	Exact identifier application number: M006
Societe Clear Skin Pads	SALICYLIC ACID	Societe Clinical Skincare	543a4347-d7d8-3050-e063-6294a90ab3a2	2026-06-16	Warnings	Exact identifier application number: M006
FHF Crisp Start	ACNE CLEANSER	Summer Soles LLC dba Farmhouse Fresh Goods	54391292-263d-253e-e063-6394a90a742f	2026-06-16	Warnings	Exact identifier application number: M006
FHF Change Peel Pads	SALICYLIC PADS	Summer Soles, LLC dba Farmhouse Fresh Goods	5439a9dd-786c-9140-e063-6394a90a8fa9	2026-06-16	Warnings	Exact identifier application number: M006
FHF Day Breakthru	SALICYLIC SERUM	Summer Doles dba Farmhouse Fresh Fresh Goods	54397bb7-1845-72a7-e063-6394a90abbd1	2026-06-16	Warnings	Exact identifier application number: M006
Societe Daily Exfoliation	SALICYLIC ACID	Societe Clinical Skincare	54633a24-3761-14d7-e063-6294a90a89f9	2026-06-16	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