Renu Laboratories Acne Sulphur L

Product NDC: 76348-450
11-digit product format: 763480450
Labeler code: 76348
Product ID: 76348-450_4616a187-4faa-181d-e063-6294a90ae910
Type: HUMAN OTC DRUG
Nonproprietary name: Acne Sulfur Lotion
Dosage form: SUSPENSION
Route: TOPICAL
Labeler: Renu Laboratories, LLC
Application: M006
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-04-16
Substance: SULFUR
Active strength: 1.4 g/14g
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 · 18 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	76348-450-02	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	76348-450-02	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	76348-450-02	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	76348-450-02	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	76348-450-02	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	76348-450-02	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	76348-450-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	76348-450-02	U	Excluded because listing certification expired	`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	76348-450-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Renu Laboratories Acne Sulphur L
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SULFUR	1.4 g/14g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
70FD1KFU70	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
240725	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
13de0e4c-b134-41c0-e054-00144ff88e88	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76348-450-02	2025-12-16	C162847	48780-1	2cef2736-7299-d83d-e063-dadaa90ab31f	Sulfur Lotion
76348-450-02	2025-01-30	C162847	48780-1	2cef2736-7299-d83d-e063-dadaa90ab31f	Sulfur Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76348-450-02	Renu Laboratories Acne Sulphur L	56 g in 1 BOTTLE, GLASS	SUSPENSION	56		6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
SULFUR	ACTIVE MOIETY	70FD1KFU70	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
CAMPHOR (SYNTHETIC)	INACTIVE INGREDIENT	5TJD82A1ET	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
MAGNESIUM ALUMINUM SILICATE	INACTIVE INGREDIENT	6M3P64V0NC	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
SALICYLIC ACID	INACTIVE INGREDIENT	O414PZ4LPZ	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76348-450	RENU LABORATORIES ACNE SULPHUR L (ACNE SULFUR LOTION) SUSPENSION [RENU LABORATORIES, INC.]	5	Current NDC, Legacy NDC, 1 package rows	20220118_13de0e4c-b134-41c0-e054-00144ff88e88.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 12 of 55 · 1,088 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acne Treatment	BENZOYL PEROXIDE	Topco Associates LLC	8d5e7e40-5e61-470a-b8ff-0b2dca3cabb0	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Daily Acne Control Cleanser	BENZOYL PEROXIDE	Topco Associates LLC	8474d917-7ee4-4d1d-8499-3520f771d2fd	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Body Wash	SALICYLIC ACID	Topco Associates LLC	1b16b978-70e0-4bba-a8d7-a77d7e1f896a	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Scrub	SALICYLIC ACID	Topco Associates LLC	e98a8184-c5a8-4306-9fff-9dc77e9d2d44	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Salicylic Acid	ASTRINGENT	Topco Associates LLC	7d15560f-d8d1-4dfe-8eca-b16bb529ad87	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	Topco Associates LLC	3149260c-b92b-43a7-8f57-897517102fa8	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Treatment	BENZOYL PEROXIDE	Walgreen Co.	07721aa6-867a-436f-8c88-ab135f02a6b5	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Scrub	SALICYLIC ACID	Amazon.com Services LLC	06339296-14e7-4179-aa2f-538bae921a8b	2026-02-11	Warnings, Adverse reactions	Exact identifier application number: M006
natouch	SALICYLIC ACID	Natouch LLC	3af85c98-f14d-5857-e063-6394a90aed13	2026-02-10	Warnings	Exact identifier application number: M006
ACNE TREATMENT	TREAT	Bio Clarity LLC	4a7e40c1-7421-a0c7-e063-6294a90a4d6b	2026-02-10	Warnings	Exact identifier application number: M006
HerbaGlow Baiwooxia Anti-Acne Gel	SALICYLIC ACID GEL	Kungpo Health Care & Herbal Center Inc	010029a3-8c1a-4f29-a162-a8ba4f939058	2026-02-10	Warnings	Exact identifier application number: M006
Acne Cleanser	BENZOYL PEROXIDE	Walmart, Inc.	04514cbb-6041-4bd5-9ab9-31312b0d8f19	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M006
Salicylic acid	SALICYLIC ACID	Topco Associates LLC	4a28800d-14ef-d841-e063-6394a90a692b	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M006
Medicated Apricot Scrub	SALICYLIC ACID	Retail Business Services, LLC	1942bd34-a152-450e-a5c5-46488da66b3d	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	American Sales Company	613f0a91-32d3-4a1e-9c9f-f0167481b511	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M006
ACNE DOTS (Skin Care Multi-Pack)	SALICYLIC ACID	Ganzhou Olivee Cosmetic Co., Ltd.	4a0dc951-07ce-2030-e063-6294a90ab2ea	2026-02-05	Warnings	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	Publix Super Markets, Inc.	169eaaa4-308d-44ba-ad93-3205e0dd9ae1	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M006
SPOTLESS Daily Acne Wash	BENZOYL PEROXIDE	Rodan & Fields	8f7bb793-3c60-4014-954e-514ef87a44fb	2026-02-04	Warnings	Exact identifier application number: M006
SPOTLESS Acne Clearing Treatment	BENZOYL PEROXIDE	Rodan & Fields	3d4ef4ce-9be3-436a-9f93-c01caa93d1a8	2026-02-04	Warnings	Exact identifier application number: M006
SPOTLESS REGIMEN FOR ACNE, BLEMISHES AND BREAKOUTS	BENZOYL PEROXIDE	Rodan & Fields	8b2c187d-4b66-4872-8243-4365ea2e8b59	2026-02-04	Warnings	Exact identifier application number: M006

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
70FD1KFU70	SULFUR	7704-34-9	SULFUR

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
240725	sulfur 10 % Topical Lotion	PSN	13de0e4c-b134-41c0-e054-00144ff88e88	6
240725	sulfur 100 MG/ML Topical Lotion	SCD	13de0e4c-b134-41c0-e054-00144ff88e88	6
240725	sulfur 10 % Topical Lotion	SY	13de0e4c-b134-41c0-e054-00144ff88e88	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76348-450-02	76348045002	56 g in 1 BOTTLE, GLASS (76348-450-02)	56 g	2015-04-16	0000-00-00	No	No	Current