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 11 of 55 · 1,088 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment	SALICYLIC ACID	SICOS ET CIE	6e366dc4-288a-47b1-ab72-8ed3aa6aea22	2026-03-02	Warnings	Exact identifier application number: M006
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment	SALICYLIC ACID	LOreal USA Products Inc	c5ce4ec6-176f-4bb0-96f0-6817e53c1468	2026-03-02	Warnings	Exact identifier application number: M006
FOLUPIA MILIA REMOVER	SALICYLIC ACID 1% MILIA REMOVER	Jiangxi Yudexi Pharmaceutical Co., LTD	4bca1a8b-2df4-47b1-e063-6394a90a33ff	2026-02-27	Warnings	Exact identifier application number: M006
Medicated Apricot Scrub	SALICYLIC ACID	Walmart Inc.	56e29d46-a29d-4192-9fdf-58dbcb843d44	2026-02-27	Warnings	Exact identifier application number: M006
Acne Treatment	BENZOYL PEROXIDE	Walmart Inc.	950edb4e-fbba-41e3-9ec5-973806e555e7	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M006
Body Wash	SALICYLIC ACID	Walmart Inc.	c31a5629-66c3-47a7-96ea-9987b2be82af	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Control Cleanser	SALICYLIC ACID	Walmart Inc.	2df52d35-dbb6-1d35-e063-6394a90ae110	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M006
Quick Action	SALICYLIC ACID	Walmart Inc.	00025ea5-d15f-49d2-a52a-6c1bd8c6a033	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	Walmart Inc.	31e49de0-0806-d18b-e063-6294a90ae47d	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M006
ACNE SOLUTIONS SPOT HEALING ACNE MEDICATION	SALICYLIC ACID	CLINIQUE LABORATORIES LLC	c09ee4f6-b8f9-4d20-982a-fb490830bd34	2026-02-26	Warnings	Exact identifier application number: M006
Acne Treatment	BENZOYL PEROXIDE	The Kroger Co.	a6526d73-4094-45b7-97f0-561dd10d61e2	2026-02-26	Warnings, Adverse reactions	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	Meijer, Inc.	29a62723-a58d-4912-bdab-b2fa1fac27b4	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M006
Medicated Apricot Scrub	SALICYLIC ACID	Meijer, Inc.	3aeb4f0b-a8f7-4ed7-b320-45e5ba0c8175	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M006
Acne Cleanser	BENZOYL PEROXIDE	Meijer, Inc.	932ee049-ab3d-4839-a655-772e5594f6e1	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M006
PHARMA CLEAR SPOT TREATMENT	SALICYLIC ACID	PHARMAGEL INTERNATIONAL INC	24736409-b500-4aae-857e-1f4fb1760a15	2026-02-19	Warnings	Exact identifier application number: M006
Acne Scrub	SALICYLIC ACID	United Natural Foods, Inc. dba UNFI	1a4df18d-8128-4846-80bc-262ba1a2aeca	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M006
Oil Free Acne Wash	SALICYLIC ACID 2%	United Natural Foods, Inc. dba UNFI	c489c818-d69a-4011-9c37-60c8c5b9522a	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M006
Medicated Apricot Scrub	SALICYLIC ACID	United Natural Foods, Inc. dba UNFI	677c19eb-780b-479b-ab1d-df249e0af6ea	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M006
PoreFect	SALICYLIC ACID	Our-Science Inc.	4afe4115-cdf0-6dd3-e063-6394a90a2453	2026-02-16	Warnings	Exact identifier application number: M006
iShancare Folliculitis Cream	FOLLICULITIS CREAM	Shenzhen Ishan Technology Co., Ltd	0c85c8e9-f50f-1b72-e063-6394a90a88c4	2026-02-13	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