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		2026-08-17

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…`

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 55 · 1,096 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
WART REMOVER	SALICYLIC ACID	Shengnan (Guangzhou) Cosmetics Co., LTD	58e901b8-66e0-d2d6-e063-6394a90ae601	2026-08-13	Warnings	Exact identifier application number: M006
BellamiLuxx Butt Acne Treatment Cream	SALICYLIC ACID 2%	BellamiLuxx LLC	42f3367f-40a2-5d97-e063-6294a90a6e33	2026-08-13	Warnings	Exact identifier application number: M006
Folliculitis Cream	MICONAZOLE NITRATE	Beautivity LLC	3155dd5e-621b-358e-e063-6294a90a90f8	2026-08-13	Warnings	Exact identifier application number: M006
WART REMOVER	SALICYLIC ACID	Shengnan (Guangzhou) Cosmetics Co., LTD	58d245c3-c685-5784-e063-6294a90a1e23	2026-08-12	Warnings	Exact identifier application number: M006
24 PK BLEMISH DOT	SALICYLIC ACID 0.5%	Ganzhou Olivee Cosmetic Co., Ltd.	66e0a0a5-22b5-4c89-a949-e996071a585b	2026-08-12	Warnings	Exact identifier application number: M006
24 PK BLEMISH DOT	SALICYLIC ACID 0.5%	Ganzhou Olivee Cosmetic Co., Ltd.	13b5a729-e265-47fd-b082-2557805d08bc	2026-08-12	Warnings	Exact identifier application number: M006
24 PK BLEMISH DOT	SALICYLIC ACID 0.5%	Ganzhou Olivee Cosmetic Co., Ltd.	9339d7ed-6e8a-48d2-a5dd-76d395e8d265	2026-08-12	Warnings	Exact identifier application number: M006
Spot Correction	SULFUR	HydroPeptide LLC	45ec40ff-7134-085b-e054-00144ff8d46c	2026-08-12	Warnings	Exact identifier application number: M006
CLERIVY MICRODART ACNE	SALICYLIC ACID	Guhada Co., Ltd.	555e0963-025e-3731-e063-6394a90a679d	2026-08-11	Warnings	Exact identifier application number: M006
Benzoyl Peroxide	BENZOYL PEROXIDE	Malezia LLC	b1304464-bd7e-fb5d-e053-2995a90a54c4	2026-08-11	Warnings	Exact identifier application number: M006
SUZANOBAGIMD Acne Cleansing Wipes	SALICYLIC ACID	Obagi Cosmeceuticals LLC	91517c5a-1653-41f3-8dfb-a9dea620765c	2026-08-10	Warnings	Exact identifier application number: M006
APUREE Prorevive Maximum Strength Antifungal	COLLOIDAL SULFUR	Guangzhou Meixi Biotechnology Co., Ltd.	58860baa-070a-7b73-e063-6294a90acdf0	2026-08-08	Warnings	Exact identifier application number: M006
DG Health Athletes Foot	TOLNAFTATE	Dolgencorp, LLC	42eb14a8-d5e0-42e1-a5a2-3f65bbfa6f3f	2026-08-07	Warnings	Exact identifier application number: M006
Acne Control Cleanser	SALICYLIC ACID	CVS Health	07cb1c7c-5188-49d5-916e-e2161b5ca3b0	2026-08-06	Warnings	Exact identifier application number: M006
PIMPLE PATCHES	PIMPLE PATCHES	Shenzhen Hengdasheng Technology Co., Ltd	584d3833-4593-94db-e063-6294a90ad3ff	2026-08-05	Warnings	Exact identifier application number: M006
Acne Clearing Sulfur Mask	SULFUR	AcneFree, LLC	c0675282-ff00-edba-e053-2995a90ace68	2026-07-31	Warnings	Exact identifier application number: M006
Sulfur Acne Foaming Cleanser	SULFUR	Acne Free, LLC	feb82a3d-cda3-c62a-e053-6394a90ad9bb	2026-07-31	Warnings	Exact identifier application number: M006
Acne Free BLACKHEAD REMOVING SCRUB 2 Salicylic Acid with Charcoal	SALICYLIC ACID	AcneFree LLC	c9393340-8a5f-6b7c-e053-2995a90afcd9	2026-07-31	Warnings	Exact identifier application number: M006
AMBI Even and Clear Exfoliating Wash Acne Treatment	SALICYLIC ACID	AMBI ENTERPRISES, LLC	43a4712d-9a6d-4bfc-abe4-f6e81dca3549	2026-07-31	Warnings	Exact identifier application number: M006
Acne Free Free 24 HR Acne Clearing System	BENZOYL PEROXIDE	AcneFree, LLC	c939847a-72eb-96fa-e053-2a95a90a4f9c	2026-07-31	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