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 34 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join ALMAY CLEAR COMPLEXION MAKEUP FOUNDATION Caramel SALICYLIC ACID ALMAY 2a982e0e-4720-797e-e063-6294a90a43c1 2024-12-31 Warnings Exact identifier application number: M006 ALMAY CLEAR COMPLEXION MAKEUP FOUNDATION Mocha SALICYLIC ACID ALMAY 2a9807d1-cf87-7096-e063-6394a90afca3 2024-12-31 Warnings Exact identifier application number: M006 ALMAY CLEAR COMPLEXION MAKEUP FOUNDATION Natural Tan SALICYLIC ACID ALMAY 2a981e22-d7d1-311b-e063-6294a90ab25f 2024-12-31 Warnings Exact identifier application number: M006 ALMAY CLEAR COMPLEXION CONCEALER SALICYLIC ACID ALMAY c3b57024-120e-390f-e053-2a95a90a6d35 2024-12-30 Warnings Exact identifier application number: M006 Almay Clear Complexion Makeup Buff SALICYLIC ACID Almay 2a83300a-15f0-365a-e063-6394a90a28d1 2024-12-30 Warnings Exact identifier application number: M006 RETINOL CLEARING SALICYLIC ACID Dermalogica, LLC. 4c20d87c-f3cf-4a40-acec-b0a8bfb9b29c 2024-12-30 Warnings Exact identifier application number: M006 Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Balm SALICYLIC ACID L'Oreal USA Products Inc 0c902cfa-d98a-42c3-967b-5a7c51a65249 2024-12-30 Warnings Exact identifier application number: M006 Salicylic Acid Cleanser EXFOLIATING AND CLARIFYING FACE WASH Bentley Laboratories, LLC eb7fa2b5-3bdb-436c-8576-1eea29b8d1ff 2024-12-27 Warnings Exact identifier application number: M006 Acne Control Superclean Body Wash AHA BHA Formula SALICYLIC ACID Bentley Laboratories, LLC 16fd3343-d044-4f6b-af1a-30bc32ce2041 2024-12-27 Warnings Exact identifier application number: M006 SkinCeuticals Blemish Plus Age Defense Acne Treatment SALICYLIC ACID L'Oreal USA Products Inc 5726d12c-708c-46e6-a584-9e5c7a544fc8 2024-12-27 Warnings Exact identifier application number: M006 SkinCeuticals Clarifying Exfoliating Cleanser SALICYLIC ACID L'Oreal USA Products Inc a0cc4ae7-c266-4321-92e6-a46d560a74b2 2024-12-27 Warnings Exact identifier application number: M006 BRODA Acne SALICYLIC ACID Bentley Laboratories, LLC b7e1f105-8998-46a5-b1ae-85d21790b816 2024-12-27 Warnings Exact identifier application number: M006 Monat Be Clarified Acne-Clearing Moisturizer SALICYLIC ACID Cosmax Usa, Corporation 2984d615-7ed1-46c3-e063-6294a90a1f8a 2024-12-26 Warnings Exact identifier application number: M006 Nativae Milia Acne Serum SALICYLIC ACID CDE BRANDS LLC e04cf0a2-bda7-4e5b-9771-769995cf6925 2024-12-26 Warnings Exact identifier application number: M006 Milani Erase Base Blemish Control Primer SALICYLIC ACID Cosmax Usa, Corporation 1b1f1948-2ad9-48d2-9871-6830b2442f43 2024-12-26 Warnings Exact identifier application number: M006 Oxy Sensitive Skin Acne Cleansing Pads SALICYLIC ACID 0.5% The Mentholatum Company 2a36b6c5-f518-66f0-e063-6394a90acd40 2024-12-26 Warnings Exact identifier application number: M006 Oxy Deep Pore Acne Cleansing Pads SALICYLIC ACID 2% The Mentholatum Company 2a385fac-399b-c111-e063-6394a90aefc3 2024-12-26 Warnings Exact identifier application number: M006 Oxy 3-IN-1 Acne Cleansing Pads SALICYLIC ACID 2% The Mentholatum Company 2a398c8d-09e6-513b-e063-6294a90ad857 2024-12-26 Warnings Exact identifier application number: M006 DEEP ACNE SULFUR Dermalogica, LLC. d4e9d230-2ee4-4cc7-a7c9-a7dde50b6f40 2024-12-26 Warnings Exact identifier application number: M006 SUNDAY RILEY SATURN SULFUR ACNE SPOT TREATMENT MASK SULFUR Sunday Riley Modern Skincare, LLC 35364a71-b011-42f5-9941-4a2f8440808b 2024-12-26 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