Home NDC 76348-450 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# 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 Uploaded 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 10 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SUFLUR SPOTandMASK Acne Clearing Treatment Mask SULFUR CA-Botana International 4d77310a-2441-a17e-e063-6394a90ae68b 2026-03-20 Warnings Exact identifier application number: M006 Daily Acne Control Cleanser BENZOYL PEROXIDE Amazon.com Services LLC 2dddc0ef-352a-4973-8402-15aecddcc43f 2026-03-20 Warnings, Adverse reactions Exact identifier application number: M006 Saltair Acne Bodyspray SALICYLIC ACID Saltair Body LLC 4d7c16a6-9b43-fbe3-e063-6294a90af051 2026-03-20 Warnings Exact identifier application number: M006 Byoma Acne Clearing Body Wash SALICYLIC ACID Byoma Ltd 2fffd6a2-1a0e-36d4-e063-6294a90ad1bc 2026-03-19 Warnings Exact identifier application number: M006 Derm Acne Solution Gel SALICYLIC ACID Yantai Aien Biotechnology Co., Ltd. 4d6c98ab-801d-63bc-e063-6294a90a20c3 2026-03-19 Warnings Exact identifier application number: M006 Sofie Pavitt Face Reset Benzoyl Peroxide Acne Treatment Mask BENZOYL PEROXIDE Cosco International, Inc. 464c0ed1-ebc4-45b1-80e3-dfe0b76312e3 2026-03-17 Warnings Exact identifier application number: M006 Neutrogena Rapid Clear Stubborn Acne Spot BENZOYL PEROXIDE Kenvue Brands LLC 5b11b2de-d156-4d6a-8024-0a945661cd9a 2026-03-12 Warnings Exact identifier application number: M006 Clean and Clear persa-gel 10 Maximum Strength BENZOYL PEROXIDE Kenvue Brands LLC c9642441-4d3a-1128-e053-2995a90aefd1 2026-03-12 Warnings Exact identifier application number: M006 14% Azelaic Acid Acne AZELAIC ACID Guangdong Bisutang Biotechnology Co., Ltd. 4ccaa734-83be-611b-e063-6294a90ab3bf 2026-03-11 Warnings Exact identifier application number: M006 Body Wash SALICYLIC ACID Amazon.com Services LLC b5d7da95-81ff-4ef9-8b80-2d046cc2a608 2026-03-10 Warnings, Adverse reactions Exact identifier application number: M006 Tula Skincare Breakout Star Lightweight Acne Moisturizer SALICYLIC ACID The Procter & Gamble Manufacturing Company 4bd1d5f5-1b3c-5e82-e063-6394a90a6454 2026-03-09 Warnings Exact identifier application number: M006 natouch SALICYLIC ACID Natouch LLC 4cb2cc1b-1793-b0c4-e063-6294a90a430f 2026-03-08 Warnings Exact identifier application number: M006 BYT BANGYTONG MILIA REMOVER SALICYLIC ACID 1% MILIA REMOVER LIQUID Shenzhen Jindali Technology Co., Ltd 4c5c3368-b3d2-976f-e063-6294a90a7046 2026-03-06 Warnings Exact identifier application number: M006 RoyceDerm Rosacea Relief Cream. SULFUR 1X HPUS 10% RoyceDerm LLC 4c3f6332-de46-f107-e063-6294a90ad63f 2026-03-04 Warnings Exact identifier application number: M006 Medicated Apricot Scrub SALICYLIC ACID Topco Associates LLC 66ccfcb7-6217-4bfb-ac11-4bcbdecb27d8 2026-03-03 Warnings, Adverse reactions Exact identifier application number: M006 Acne Treatment BENZOYL PEROXIDE Amazon.com Services LLC 08c28255-a223-416e-a2d9-ecb149b0f051 2026-03-03 Warnings, Adverse reactions Exact identifier application number: M006 Neutrogena Evenly Clear Acne Gel Moisturizer SALICYLIC ACID Kenvue Brands LLC 3f8f344d-a468-8eb3-e063-6394a90a7dd7 2026-03-02 Warnings Exact identifier application number: M006 Acne Scrub SALICYLIC ACID Old East Main Co. f63d4184-44a2-484f-ae51-ce37e19374a2 2026-03-02 Warnings, Adverse reactions Exact identifier application number: M006 Acne Wash SALICYLIC ACID Old East Main Co. 7bf6f18f-a1ec-460e-afbc-51be1add05b6 2026-03-02 Warnings, Adverse reactions Exact identifier application number: M006 Advanced DermaClear Serum SALICYLIC ACID Allure Labs 4c10bc9a-52b0-fbf2-e063-6394a90a5780 2026-03-02 Warnings Exact identifier application number: M006
DailyMed RxNorm Mappings# 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